反应 #1880969

ord-38985094ddf44896be42573da557fafc

反应方程式

CCOC(=O)[C@@H]1CCCN1C(=O)C(CC)CC
N-(2-ethylbutyryl)-2(S)-pyrrolidine-carboxylic acid ethylester
[Na+].[OH-]
NaOH
Cl
HCl
CCC(CC)C(=O)N1CCC[C@H]1C(=O)O
desired product
收率 104.6%
CCC(CC)C(=O)N1CCC[C@H]1C(=O)O
N-(2-Ethylbutyryl)-2(S)-pyrrolidine-carboxylic acid
收率 104.6%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was cooled on ice-bath
  2. 2
    浓缩The reaction mixture was concentrated in vacuo
  3. 3
    workup.DISSOLUTIONthe residue was dissolved in chloroform
  4. 4
    洗涤washed with water
  5. 5
    干燥dried over anhydrous sodium sulfate
  6. 6
    其他The solvents were removed in vacuo

实验过程

To methanol solution (13 ml) of N-(2-ethylbutyryl)-2(S)-pyrrolidine-carboxylic acid ethylester 1.46 g (6.05 mmol), 2N—NaOH solution (6.5 ml) was added, and stirring was continued at room temperature for 2 hours. The reaction mixture was cooled on ice-bath, and adjusted to pH2 with 6N—HCl solution. The reaction mixture was concentrated in vacuo, and the residue was dissolved in chloroform, washed with water, and then dried over anhydrous sodium sulfate. The solvents were removed in vacuo to yield 1.35 g of desired product as an oil. NMR was consistent with the desired title product.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07022677B1uspto-grants-2006_04