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Dimethyl Sulfoxide → Benzyl (2-oxobutyl)carbamate

HRID 1385185
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HRID 1385185 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([O:18][C:19]([NH:21][CH2:22][CH:23]([OH:26])[CH2:24][CH3:25])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>C(Cl)Cl>[CH2:11]([O:18][C:19]([NH:21][CH2:22][C:23](=[O:26])[CH2:24][CH3:25])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
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6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 18667998benzyl N-(2-hydroxybutyl)carbamate

생성물 1

HCID 18667993Benzyl (2-oxobutyl)carbamate수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
-78 °C

실험 절차

To methylene chloride (60 mL) at −78° C. under argon was added oxalyl chloride (37 mL of 2 M solution in methylene chloride, 74 mmol), followed by DMSO (7.8 g, 100 mmol). The mixture was stirred at −78° C. for 20 min. and to this mixture was added a solution of 1-benzyloxycarbonylamino-2-butanol (13.9 g, 61.8 mmol) in methylene chloride (40 mL). The mixture was stirred at −78° C. for 1 h and triethylamine (21 mL) was added to the mixture. It was warmed to room temperature (rt) and washed successively with 1 N hydrochloric acid and aqueous sodium bicarbonate solution. The methylene chloride solution was dried over MgSO4 and concentrated to afford 1-15 benzyloxycarbonylamino-2-butanone (11.2 g, 82%) as a solid, which was enough pure for the next reaction.

후처리

  1. stirringThe mixture was stirred at −78° C. for 1 h
  2. temperatureIt was warmed to room temperature (rt)
  3. washwashed successively with 1 N hydrochloric acid and aqueous sodium bicarbonate solution
  4. dry with materialThe methylene chloride solution was dried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a08ece5bd02c411fb22ad7552b114ca7
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06262096B1

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