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Potassium Hydroxide → Boc-D-Met-Gly-OH

HRID 746228
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HRID 746228 반응식
C[O:2][C:3](=[O:21])[CH2:4][NH:5][C:6](=[O:20])[C@@H:7]([CH2:16][CH2:17][S:18][CH3:19])[NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10].[OH-].[K+]>CO>[C:12]([O:11][C:9]([NH:8][C@@H:7]([C:6]([NH:5][CH2:4][C:3]([OH:21])=[O:2])=[O:20])[CH2:16][CH2:17][S:18][CH3:19])=[O:10])([CH3:15])([CH3:13])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 13216971methyl Boc-D-methionyl-glycinate

생성물 1

HCID 7019049Boc-D-Met-Gly-OH

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The title compound of Example 8 (32.0 g, 0.1 mole) was dissolved in 200 ml of methanol to which was added 200 ml of 2 M potassium hydroxide. After ca. 5 min. at room temperature the solution was concentrated to about half volume and diluted with ethyl acetate. The solution was neutralized by washing with two portions of 0.5 M potassium bisulfate, and then dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product was recrystallized to give the title compound, which was used in subsequent reactions without further purification.

후처리

  1. concentrationAfter ca. 5 min. at room temperature the solution was concentrated to about half volume
  2. additiondiluted with ethyl acetate
  3. washby washing with two portions of 0.5 M potassium bisulfate
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude product was recrystallized

출처 및 근거

ORD 기록
ord-420658556cdf405d9fff39ed9d8c50c3
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04603121

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