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Benzoyl chloride, 3,4-dichloro- → HCID 21409861, 화합물

HRID 2071993
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HRID 2071993 반응식
[CH3:1][NH:2][CH2:3][C:4]1([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.[Cl:16][C:17]1[CH:18]=[C:19]([CH:23]=[CH:24][C:25]=1[Cl:26])[C:20](Cl)=[O:21]>C1C=CC=CC=1>[ClH:16].[CH3:1][N:2]([CH2:3][C:4]1([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)[C:20](=[O:21])[C:19]1[CH:23]=[CH:24][C:25]([Cl:26])=[C:17]([Cl:16])[CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 76403Benzoyl chloride, 3,4-dichloro-HCID 21409890N-Methyl-1-[1-(piperidin-1-yl)cyclohexyl]methanamine

생성물 1

HCID 21409861HCID 21409861, 화합물

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

Solutions of 1-[1-[(methylamino)methyl]cyclohexyl] piperidine (1.1 g., 0.005 mole) in dry benzene (25 ml) and 3,4-dichlorobenzoyl-chloride (1.0 g., 0.005 mole) in dry benzene (50 ml) were mixed and heated under reflux (steam bath) for 1 hr. The precipitate was filtered washed with benzene and dried. (1. 6 g.) m.p. 222° (dec.)

후처리

  1. temperatureheated
  2. temperatureunder reflux (steam bath) for 1 hr
  3. filtrationThe precipitate was filtered
  4. washwashed with benzene
  5. customdried

출처 및 근거

ORD 기록
ord-e0f7b7a397ee4f8db7658706442f6d2c
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04049663

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