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Benzyl chloroformate → HCID 60204906, 화합물

HRID 1245034
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HRID 1245034 반응식
C(=O)([O-])O.[Na+].Cl[C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8].[CH3:17][O:18][C:19](=[O:26])[C@@H:20]1[CH2:24][CH:23]([CH3:25])[CH2:22][NH:21]1>C1(C)C=CC=CC=1>[CH3:17][O:18][C:19](=[O:26])[C@@H:20]1[CH2:24][CH:23]([CH3:25])[CH2:22][N:21]1[C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10387Benzyl chloroformateHCID 516892Sodium BicarbonateHCID 45089984HCID 45089984, 화합물

생성물 1

HCID 60204906HCID 60204906, 화합물수율 99%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

20 ml of an aqueous solution containing 1.89 g (22.5 mmol) of sodium hydrogencarbonate and 1.54 ml (10.8 mmol) of benzyl chloroformate were added to a solution of 0.93 g (6.5 mmol) of (2S)-4-methylproline methyl ester [obtained as described in Preparative Example 8(ii)′ above] in 20 ml of toluene, and the resulting mixture was stirred at room temperature over night. At the end of this time, the reaction mixture was extracted with ethyl acetate. The organic extract was washed with water and concentrated under reduced pressure to afford 1.78 g (yield: 99%) of (2S)-1-benzyloxycarbonyl-4-methylproline methyl ester as a pale yellow oil. Subsequently, all of the compound thus obtained was reduced using lithium borohydride, in a similar manner to that described in Preparative Example 5(i)′ above, to afford 1.07 g (yield: 66%) of the title compound as a pale yellow oil.

후처리

  1. customobtained
  2. extractionAt the end of this time, the reaction mixture was extracted with ethyl acetate
  3. extractionThe organic extract
  4. washwas washed with water
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a546b5f1ac6d4bee8327040ac9a6e78f
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07122666B2

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