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Cyclopropanecarbonyl chloride → HCID 20314164, 화합물

HRID 2419639
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HRID 2419639 반응식
[F:1][C:2]([F:21])([F:20])[C:3]([C:16]([F:19])([F:18])[F:17])([C:5]1[CH:6]=[CH:7][C:8]2[NH:14][CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[CH:15]=1)[OH:4].[CH:22]1([C:25](Cl)=[O:26])[CH2:24][CH2:23]1>C1(C)C=CC=CC=1>[CH:22]1([C:25]([N:14]2[C:8]3[CH:7]=[CH:6][C:5]([C:3]([C:2]([F:1])([F:20])[F:21])([C:16]([F:19])([F:17])[F:18])[OH:4])=[CH:15][C:9]=3[CH2:10][CH2:11][CH2:12][CH2:13]2)=[O:26])[CH2:24][CH2:23]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 77637Cyclopropanecarbonyl chlorideHCID 23346095alpha,alpha-bis(trifluoromethyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-7-methanol

생성물 1

HCID 20314164HCID 20314164, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To 200 ml dry toluene is added 6.3 g (0.020 mole) α,α-bis(trifluoromethyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-7-methanol and 3.0 g (0.025 mole) cyclopropane carboxylic acid chloride. The solution is stirred and heated at reflux under nitrogen for sixteen hours, then cooled and evaporated at reduced pressure. The residual solid is recrystallized from chlorobutane to give 5.0 g, m.p. 165°-167°.

후처리

  1. temperatureheated
  2. temperatureat reflux under nitrogen for sixteen hours
  3. temperaturecooled
  4. customevaporated at reduced pressure
  5. customThe residual solid is recrystallized from chlorobutane
  6. customto give 5.0 g, m.p. 165°-167°

출처 및 근거

ORD 기록
ord-ed16f582762e42bc9b06fac8ef7463c3
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04107303

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