摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

S-phenyl 3-hydroxy-2-methyl-3-phenylthiopropanoate | 52411-61-7

中文名称
——
中文别名
——
英文名称
S-phenyl 3-hydroxy-2-methyl-3-phenylthiopropanoate
英文别名
S-phenyl 3-hydroxy-2-methyl-3-phenylpropanethioate
S-phenyl 3-hydroxy-2-methyl-3-phenylthiopropanoate化学式
CAS
52411-61-7
化学式
C16H16O2S
mdl
——
分子量
272.368
InChiKey
SYHUSISPSSCAFY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.68
  • 重原子数:
    19.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    37.3
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    S-phenyl 3-hydroxy-2-methyl-3-phenylthiopropanoate 在 lithium aluminium tetrahydride 、 三乙胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 生成 Methanesulfonic acid (2S,3R)-3-hydroxy-2-methyl-3-phenyl-propyl ester
    参考文献:
    名称:
    The stereoselective synthesis of oxetanes; exploration of a new, Mitsunobu-style procedure for the cyclisation of 1,3-diols
    摘要:
    一种2-甲基-3-[1-(芳基硫)环己基]丙烷-1,3-二醇1在甲苯中与三苯基膦、Ziram® 2和DEAD反应,产物为3-甲基-2-[1-(芳基硫)环己基]噁烯3,产率为85%。我们进行了机理研究,找到了最佳反应条件,并探索了该反应适用的底物范围。我们还包括了一项X射线研究的结果,该研究显示化合物33(醇1的氧化产物)是磺酮而非先前报告的亚磺酸盐。
    DOI:
    10.1039/b106851b
  • 作为产物:
    参考文献:
    名称:
    HIRAMA MASAHIRO; GARVAY D. S.; LU L. D.-L.; MASAMUNE SATORU, TETRAHEDRON LETT., 1979, NO 41, 3137-3140
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Practical enantioselective Diels-Alder and aldol reactions using a new chiral controller system
    作者:E. J. Corey、Rene Imwinkelried、Stanislaw Pikul、Yi Bin Xiang
    DOI:10.1021/ja00196a081
    日期:1989.7
    Catalyse par le complexe cyclique Al [−N(SO 2 CF 3 )(CHPh) 2 (CF 3 SO 2 )N-] R, R=i-Bu, CH 3
    催化par le complexe cyclique Al [-N(SO 2 CF 3 )(CHPh) 2 (CF 3 SO 2 )N-] R, R=i-Bu, CH 3
  • A CONVENIENT METHOD FOR THE PREPARATION OF β-HYDROXY THIOLESTERS AND ESTERS
    作者:Katsuhiko Inomata、Tatsuo Kawahara、Teruaki Mukaiyama
    DOI:10.1246/cl.1974.245
    日期:1974.3.5
    It was found that thioboronite reacted with substituted ketene (produced from α-haloacyl halide and zinc dust) and carbonyl compounds to give the corresponding α-substituted β-hydroxyalkanethioates in good yields. Also, it was established that β-hydroxyalkanoates were obtained in good yields by utilizing aluminum alkoxide in place of thioboronite in the above reaction.
    发现硼酸盐与取代的乙烯酮(由α-卤代酰卤粉产生)和羰基化合物反应,以良好的收率得到相应的α-取代的β-羟基烷烃。此外,已确定通过在上述反应中使用烷氧基铝代替硼酸盐以良好的收率获得β-羟基链烷酸酯。
  • Stereoselective aldol condensations via enolboronates.
    作者:Cesare Gennari、Silvia Cardani、Lino Colombo、Carlo Scolastico
    DOI:10.1016/s0040-4039(01)80233-1
    日期:1984.1
    Enolboronates, new enolates directly accessible from carbonyl compounds, exhibit extraordinary high erythro diastereoselection both with aliphatic and aromatic aldehydes.
    烯醇硼酸酯是可直接从羰基化合物中获得的新烯酸酯,与脂肪族和芳香族醛类均表现出非同寻常的高赤型非对映选择性。
  • A Facile and Efficient Direct Aldol Addition of Simple Thioesters
    作者:Julianne M. Yost、Guoqiang Zhou、Don M. Coltart
    DOI:10.1021/ol060413q
    日期:2006.3.1
    Simple thioesters undergo direct aldol addition to aldehydes in the presence of MgBr2.OEt2 and i-Pr2NEt using untreated, reagent-grade CH2Cl2 under atmospheric conditions. The reactions proceed extremely rapidly and in excellent yield.
查看更多

同类化合物

硬脂酸对甲苯硫酯 硫基丙酸苯酯 硫代乙酸S-[4-[二(2-氯乙基)氨基]苯基]酯 硫代乙酸 S-(2-乙基苯基)酯 乙硫酸,[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]-,S-苯基酯 丙硫酸,S-(2-甲氧苯基)酯 S1,S2-二(4-氯苯基)乙烷二(硫代ate) S-苯基硫代异丁酸酯 S-苯基3-羟基硫代丁酸酯 S-苯基2-氟硫代乙酸酯 S-硫代乙酸苯酯 S-氯乙酰基-P-巯基甲苯 S-丙酰基-p-疏基甲苯 S-[4-[2-[4-(2-苯乙炔基)苯基]乙炔基]苯基]硫代乙酸酯 S-(三氟乙酰基)-4-疏基甲苯 S-(4-甲基苯基)硫代乙酸酯 S,S′-[1,4-亚苯基二(2,1-乙炔二基-4,1-亚苯基)]双(硫代乙酸酯) O-乙基S-(4-甲基苯基)单硫代草酸酯 4-溴苯基硫代乙酸酯 4-(S-乙酰基硫代)苯甲醛 4,4-二甲基-1-氧代-1-(苯基硫基)-2-戊烷基乙酸酯 3-氧代-3-(4-甲氧基苯氧基)丙酸 2-甲基苯硫酚乙酸酯 2-(氯甲酰基)-1-环戊烯-1-基硫氰酸酯 1-乙酰巯基-4-碘苯 S-(p-tolyl) cyclohexanecarbothioate 4-(2,5-Dioxo-pyrrolidin-1-yl)-thiobutyric acid S-phenyl ester S-phenyl 2-[(S)-[(2-methylpropan-2-yl)oxycarbonylamino]-phenylmethyl]-3-oxobutanethioate Tribromthioessigsaeure-phenylester Thiocrotonsaeure-S-<4-chlor>-phenylester (4S)-4-<(Z)-3-Acetoxy-2-phenylthio-2-propenoyl>-2,2-dimethyl-1,3-dioxolane (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-tert-butyl-phenyl) ester trans-dichlorobis(thio-L-leucine-S-phenylester-N)platinum(II) 2,3,4,5,5-Pentachlor-2,4-pentadienthiosaeure-S-(4-tolyl)ester (2Z)-2,3,4,5-tetrachloro-5-(p-tolylthio)penta-2,4-dienoyl chloride (Z)-1,3-bis(phenylthio)-5-hydroxy-2-penten-1-one (2Z,4E)-2,3,4,5-Tetrachloro-5-(4-chloro-phenylsulfanyl)-penta-2,4-dienoyl chloride S-phenyl 2-diazoethanethioate (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-chloro-phenyl) ester Dithiocarbonic acid S-pentachlorophenyl ester S-phenyl ester Phenyl-α-phenylacetothiol-acetat S-(2,3,4,5,6-pentachlorophenyl) (2Z)-2,3,4,5,5-pentachloropenta-2,4-dienethioate tert-butyl 2-methyl-3-oxo-3-(phenylthio)propanoate (2Z,4E)-2,3,4,5-tetrachloro-5-(phenylthio)penta-2,4-dienoyl chloride (Z)-2,3,5,5-Tetrachlor-4-phenylthio-2,4-pentadienthiosaeure-S-phenylester (Z)-2,3,4,5-Tetrachlor-5-methylthio-2,4-pentadienthiosaeure-S-pentachlorphenylester tridecanethioic acid S-phenyl ester 1,4-bis[4-(acetylsulfanyl)phenylethynyl]-2,6-di-t-butylbenzene phenyl 2,3,4,6-tetradeoxy-4-(acetylthio)-1-thio-α-D-erythro-hex-2-enopyranoside