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

HRID 3786
ノート
印刷プレビュー

反応式

HRID 3786 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 7019049Boc-D-Met-Gly-OH

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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 2M 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 0.5M 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.

後処理

  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 0.5M potassium bisulfate
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude product was recrystallized

出典と根拠

ORDレコード
ord-37b5bfcf3c62463e96183b6c7a43b894
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04722922

反応ノート

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