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Ethyl chloroformate → 1-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline

HRID 2419429
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반응식

HRID 2419429 반응식
Cl[C:2]([O:4][CH2:5][CH3:6])=[O:3].[SH:7][CH2:8][CH2:9][C:10]([N:12]1[CH2:19][CH2:18][CH2:17][C@H:13]1[C:14]([OH:16])=[O:15])=[O:11]>C(=O)(O)[O-].[Na+]>[CH2:5]([O:4][C:2]([S:7][CH2:8][CH2:9][C:10]([N:12]1[CH2:19][CH2:18][CH2:17][C@H:13]1[C:14]([OH:16])=[O:15])=[O:11])=[O:3])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10928Ethyl chloroformateHCID 999781-(3-Mercapto-1-oxopropyl)-L-proline

생성물 1

HCID 537685991-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline

시약·촉매·용매 1

HCID 516892Sodium Bicarbonate용매

실험 절차

Ethyl chloroformate (1.2 g.) is added to a solution of 3-mercaptopropanoyl-L-proline (2.03 g.) in normal sodium bicarbonate (30 ml.) and the mixture is stirred vigorously at 5° for one hour, and for two hours at room temperature. After acidification with concentrated hydrochloric acid, the mixture is extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate, and concentrated to dryness to yield 1-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline.

후처리

  1. waitfor two hours at room temperature
  2. extractionAfter acidification with concentrated hydrochloric acid, the mixture is extracted with ethyl acetate
  3. washThe organic phase is washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-f70559b38f554c36b75b2e42e2dd3825
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04105776

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