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Triethylamine → Allyl-(1-methyl-pent-4-enyl)-carbamic acid benzyl ester

HRID 229792
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반응식

HRID 229792 반응식
[C:1](Cl)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[CH2:12]([NH:15][CH:16]([CH3:21])[CH2:17][CH2:18][CH:19]=[CH2:20])[CH:13]=[CH2:14].C(N(CC)CC)C>C(Cl)Cl>[CH2:4]([O:3][C:1](=[O:2])[N:15]([CH2:12][CH:13]=[CH2:14])[CH:16]([CH3:21])[CH2:17][CH2:18][CH:19]=[CH2:20])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10387Benzyl chloroformateHCID 11788335Allyl-(1-methyl-pent-4-enyl)-amine

생성물 1

HCID 11608774Allyl-(1-methyl-pent-4-enyl)-carbamic acid benzyl ester수율 65.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Carbobenzyloxy chloride (9.56 g, 8 ml) was added dropwise to a stirred solution of allyl-(1-methyl-pent-4-enyl)-amine (7 g, 50 mmol), triethylamine (5.5 g, 8.0 ml, 57.5 mmol) in CH2Cl2 (100 ml) at 0 C. The reaction mixture was warmed to RT, then was stirred for 2 h. The reaction mixture was diluted with CH2Cl2 (100 ml), then was extracted with water, then brine. The combined organics were dried with MgSO4, filtered, concentrated in vacuo by rotary evaporation, then was chromatographed (silica gel, 4% EtOAc/hexanes) to give the title compound (8.9 g, 65% yield): Liquid Chromatgraphy/Electrospray mass spec: M+H+=274.2

후처리

  1. extractionwas extracted with water
  2. dry with materialThe combined organics were dried with MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo by rotary evaporation
  5. customwas chromatographed (silica gel, 4% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-3470cd821f694def8a3bc8cca5535f0e
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07563784B2

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