3-Methoxycarbonylamino-butyric acid tert-butyl ester | 116173-70-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 3-Methoxycarbonylamino-butyric acid tert-butyl ester
• 英文别名: Tert-butyl 3-[(methoxycarbonyl)amino]butanoate；tert-butyl 3-(methoxycarbonylamino)butanoate
• CAS: 116173-70-7
• 化学式: C₁₀H₁₉NO₄
• mdl: MFCD24393754
• 分子量: 217.265
• InChiKey: KKAJRWXDJDJPKC-UHFFFAOYSA-N

物化性质

• 沸点：
  302.8±25.0 °C(Predicted)
• 密度：
  1.035±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  64.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  醋酸叔丁酯 、 (1-methoxy-ethyl)-carbamic acid methyl ester 在 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 2.0h， 以78%的产率得到3-Methoxycarbonylamino-butyric acid tert-butyl ester
  参考文献：
  名称：

  New synthesis of β-amino acids by nucleophilic addition of enolate anions to N-methoxycarbonylimines generated from α-methoxy carbamates1

  摘要：

  DOI：

  10.1016/s0040-4039(00)80062-3

文献信息

• Reaction of N-acyl-α-methoxyamines with organozinc reagents. A convenient method for the synthesis of homoallylamines and β-amino esters
  作者：Naoki Kise、Hiroki Yamazaki、Toshirou Mabuchi、Tatsuya Shono

  DOI：10.1016/s0040-4039(00)76758-x

  日期：1994.3

  The reaction of N-acyl-alpha-methoxyamines with allyl-, propargyl-, and benzylzinc bromides and Reformatsky reagents proceeds in THF at room temperature. Homoallyl- and homopropargylamines and beta-amino esters are synthesized in good yields.
• A New Method for the Synthesis of β-Amino Acid Derivatives and β-Lactams. Reaction of <i>N</i>-Alkoxycarbonyl-1-methoxyamines with Esters
  作者：Naoki Kise、Nasuo Ueda

  DOI：10.1021/jo990821q

  日期：1999.10.1

  The reaction of N-alkoxycarbonyl-1-methoxyamines with esters is an alternative to the reaction of imines with esters for the synthesis of beta-amino acid derivatives. In this reaction, N-alkoxycarbony-1-methoxyamines corresponding to unstable imines can also be employed. Although anti adducts were obtained preferentially in the absence of Ti complexes, the diastereoselectivity of this reaction was reversed by the addition of Ti(OPr-i)(4). The obtained adducts were transformed to the corresponding beta-lactams.
• Kise Naoki, Yamazaki Hiroki, Mabuchi Toshirou, Shono Tatsuya, Tetrahedron Lett, 35 (1994) N 10, S 1561-1564
  作者：Kise Naoki, Yamazaki Hiroki, Mabuchi Toshirou, Shono Tatsuya

  DOI：——

  日期：——
• SHONO, TATSUYA;KISE, NAOKI;SANDA, FUMIO;OHI, SATORU;TSUBATA, KENJI, TETRAHEDRON LETT., 29,(1988) N 2, 231-234
  作者：SHONO, TATSUYA、KISE, NAOKI、SANDA, FUMIO、OHI, SATORU、TSUBATA, KENJI

  DOI：——

  日期：——
• US5518903A
  申请人：——

  公开号：US5518903A

  公开（公告）日：1996-05-21