[(2S,3S)-3-(phenylmethoxymethyl)oxiran-2-yl]methyl 4-methylbenzenesulfonate | 147127-70-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: [(2S,3S)-3-(phenylmethoxymethyl)oxiran-2-yl]methyl 4-methylbenzenesulfonate
• CAS: 147127-70-6
• 化学式: C₁₈H₂₀O₅S
• 分子量: 348.42
• InChiKey: BFDSNKKZNNGYAI-ROUUACIJSA-N

物化性质

• 沸点：
  504.4±30.0 °C(predicted)
• 密度：
  1.249±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  24
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  73.5
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  [(2S,3S)-3-(phenylmethoxymethyl)oxiran-2-yl]methyl 4-methylbenzenesulfonate 在 sodium hydroxide 、 碲化氢 、 sodium formaldehyde sulfoxylate 作用下， 以 四氢呋喃 为溶剂， 以87%的产率得到1-(苄氧基)丁-3-烯-2-醇
  参考文献：
  名称：

  A tellurium transposition route to allylic alcohols: overcoming some limitations of the Sharpless-Katsuki asymmetric epoxidation

  摘要：

  Good yields of enantiomeric allylic alcohols can be obtained in high enantiomeric excess (ee) by combining the Sharpless-Katsuki asymmetric epoxidation process (SAE) with tellurium chemistry. The advantages of the tellurium process are as follows: (1) the 50% yield limitation on the allylic alcohol in the Sharpless kinetic resolution (SKR) can be overcome; (2) allylic tertiary alcohols which are unsatisfactory substrates in the SKR can be obtained in high optical purity; (3) optically active secondary allylic alcohols with tertiary alkyl substituents (e.g. tert-butyl) at C-1 can be obtained in high ee; (4) optically active sterically congested cis secondary alcohols can be obtained in high ee; and (5) the nuisance of the slow SAE of some vinyl carbinols can be avoided. The key step in the reaction sequence is either a stereospecific 1,3-trans position of double bond and alcohol functionalities or an inversion of the alcohol configuration with concomitant deoxygenation of the epoxide function in epoxy alcohols. Trans secondary allylic alcohols can be converted to cis secondary allylic alcohols by way of erythro epoxy alcohols (glycidols); threo glycidyl derivatives are converted to trans secondary allylic alcohols. These transformations are accomplished by the action of telluride ion, generated in situ from the element, on a glycidyl sulfonate ester. Reduction of elemental Te is conveniently done with rongalite (HOCH2SO2Na) in an aqueous medium. This method is satisfactory when Te2- is required to attack a primary carbon site of a glycidyl sulfonate. In cases where Te2- is required to attack a secondary carbon site, reduction of the tellurium must be done with NaBH4 or LiEt3BH. Elemental tellurium is precipitated during the course of the reactions and can be recovered and reused.

  DOI：

  10.1021/jo00055a029
• 作为产物：
  描述：

  (E)-4-(benzyloxy)-2-buten-1-ol 在 titanium(IV) isopropylate 、 叔丁基过氧化氢 、 4-二甲氨基吡啶 、 L-(+)-酒石酸二异丙酯 、 4 A molecular sieve 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 [(2S,3S)-3-(phenylmethoxymethyl)oxiran-2-yl]methyl 4-methylbenzenesulfonate
  参考文献：
  名称：

  A tellurium transposition route to allylic alcohols: overcoming some limitations of the Sharpless-Katsuki asymmetric epoxidation

  摘要：

  Good yields of enantiomeric allylic alcohols can be obtained in high enantiomeric excess (ee) by combining the Sharpless-Katsuki asymmetric epoxidation process (SAE) with tellurium chemistry. The advantages of the tellurium process are as follows: (1) the 50% yield limitation on the allylic alcohol in the Sharpless kinetic resolution (SKR) can be overcome; (2) allylic tertiary alcohols which are unsatisfactory substrates in the SKR can be obtained in high optical purity; (3) optically active secondary allylic alcohols with tertiary alkyl substituents (e.g. tert-butyl) at C-1 can be obtained in high ee; (4) optically active sterically congested cis secondary alcohols can be obtained in high ee; and (5) the nuisance of the slow SAE of some vinyl carbinols can be avoided. The key step in the reaction sequence is either a stereospecific 1,3-trans position of double bond and alcohol functionalities or an inversion of the alcohol configuration with concomitant deoxygenation of the epoxide function in epoxy alcohols. Trans secondary allylic alcohols can be converted to cis secondary allylic alcohols by way of erythro epoxy alcohols (glycidols); threo glycidyl derivatives are converted to trans secondary allylic alcohols. These transformations are accomplished by the action of telluride ion, generated in situ from the element, on a glycidyl sulfonate ester. Reduction of elemental Te is conveniently done with rongalite (HOCH2SO2Na) in an aqueous medium. This method is satisfactory when Te2- is required to attack a primary carbon site of a glycidyl sulfonate. In cases where Te2- is required to attack a secondary carbon site, reduction of the tellurium must be done with NaBH4 or LiEt3BH. Elemental tellurium is precipitated during the course of the reactions and can be recovered and reused.

  DOI：

  10.1021/jo00055a029

文献信息

• One-pot transformation of p-toluenesulfonates of 2,3-epoxy alcohols into allyic alcohols
  作者：Hiromu Habashita、Takeshi Kawasaki、Masako Akaji、Hirokazu Tamamura、Tetsutaro Kimachi、Nobutaka Fujii、Toshiro Ibuka

  DOI：10.1016/s0040-4039(97)10208-8

  日期：1997.12

  efficient method for the synthesis of synthetically useful non-racemic allylic alcohols from 4-methylbenzenesulfonates of non-racemic 2,3-epoxy alcohols is described. Satisfactory yields are obtained by treatment of 4-methylbenzenesulfonates of non-racemic 2,3-epoxy alcohols with potassium iodide followed by zinc powder and ammonium chloride in a one-pot manner. The method has been successfully applied to

  描述了一种由非外消旋2，3-环氧醇的4-甲基苯磺酸酯合成合成有用的非外消旋烯丙基醇的简便有效的方法。通过用碘化钾，然后一锅法用锌粉和氯化铵处理非外消旋2,3-环氧醇的4-甲基苯磺酸盐，获得令人满意的收率。该方法已成功应用于C 30 30C 37葡萄球菌的关键构件的合成。
• Simple one-pot transformations of toluene-p-sulfonates of 2,3-epoxy alcohols into allylic alcohols
  作者：Nobutaka Fujii、Hiromu Habashita、Masako Akaji、Kazuo Nakai、Toshiro Ibuka、Masahiro Fujiwara、Hirokazu Tamamura、Yoshinori Yamamoto

  DOI：10.1039/p19960000865

  日期：——

  A simple synthetic method for the preparation of scalemic allylic alcohols from toluene-p-sulfonates of scalemic 2,3-epoxy alcohols is reported. Satisfactory yields are obtained by treatment of toluene-p-sulfonates of 2,3-epoxy alcohols with potassium iodide followed by triphenylphosphine and iodine in a one-pot synthesis.

  报道了一种简单的合成方法，该方法由规模化的2,3-环氧醇的甲苯-对-磺酸盐制备规模化的烯丙醇。通过一锅合成法，先用碘化钾，然后用三苯基膦和碘处理碘化2,3-环氧醇的甲苯对磺酸酯，可获得令人满意的收率。