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L-Methionine → Cbz-L-methionine methyl ester

HRID 2371332
ノート
印刷プレビュー

反応式

HRID 2371332 の反応式
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[CH2:3][CH2:4][S:5][CH3:6].[C:10](=O)(O)O.[Na].Cl[C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]>CCOC(C)=O.O>[CH3:10][O:8][C:7](=[O:9])[C@@H:2]([NH:1][C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17])[CH2:3][CH2:4][S:5][CH3:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6137L-MethionineHCID 10387Benzyl chloroformateHCID 24192197Carbonic acid, sodium salt

生成物 1

HCID 11141035Cbz-L-methionine methyl ester

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒

実験手順

L-methionine (3.70 g, 18.5 mmol) was dissolved in a biphasic mixture of EtOAc (75 mL) and water (75 mL). This was cooled in ice and sodium hydrogen bicarbonate (7.78 g, 5 equiv) and benzyl chloroformate (2.98 mL, 1.1 equiv) were added. This was stirred in ice for one h and then at rt for a further eighteen h before the mixture was allowed to partition. The organic phase was washed sequentially with 1M hydrochloric acid, saturated aqueous sodium hydrogen bicarbonate and brine before being dried (MgSO4), filtered and concentrated in vacuo to afford a yellow oil, 5.40 g, 98%.

後処理

  1. temperatureThis was cooled in ice
  2. customat rt
  3. customto partition
  4. washThe organic phase was washed sequentially with 1M hydrochloric acid, saturated aqueous sodium hydrogen bicarbonate and brine
  5. dry with materialbefore being dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customto afford a yellow oil, 5.40 g, 98%

出典と根拠

ORDレコード
ord-7e458bc07f8e4fd492e5bf2c3483b50d
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08710178B2

反応ノート

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