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Sodium Carbonate → N-[(benzyloxy)carbonyl]-3-methylvaline

HRID 910011
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HRID 910011 반응식
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([CH3:6])([CH3:5])[CH3:4].C([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].C([O-])([O-])=O.[Na+].[Na+]>O>[CH2:19]([O:18][C:16]([NH:1][CH:2]([C:3]([CH3:6])([CH3:5])[CH3:4])[C:7]([OH:9])=[O:8])=[O:17])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
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참가 물질

6

반응물 4

HCID 10340Sodium CarbonateHCID 10387Benzyl chloroformateHCID 164608L-tert-LeucineHCID 516892Sodium Bicarbonate

생성물 1

HCID 3401206N-[(benzyloxy)carbonyl]-3-methylvaline수율 817.3%

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

To a solution of L-tert-leucine (1) (50.0 g, 38.0 mmol) and NaHCO3 (96.0 g, 114 mmol) in ice (500 g) and water (500 ml) was added benzyl chloroformate (65.0 ml, 74.0 mmol) and the reaction stirred at 0° C. for 3 hours then at room temperature for 18 hours. 0.1N Na2CO3 was added until the oily layer dissolved and the solution was washed with 10% EtOAc in hexanes (2×500 ml). The iced aqueous phase was acidified to pH 1 using 12N HCl then extracted using EtOAc (3×350 ml). The combined organic extracts were dried over Na2SO4, filtered and evaporated to give the title compound as a colorless oil (82.4 g, 81.5% yield):

후처리

  1. waitat room temperature for 18 hours
  2. dissolutiondissolved
  3. washthe solution was washed with 10% EtOAc in hexanes (2×500 ml)
  4. extractionthen extracted
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-e82e7558dcee421b93289ae5e2df93bb
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022041B2

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