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Benzoyl chloride, 3,4-dichloro- → HCID 21409887, 화합물

HRID 2072008
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HRID 2072008 반응식
[CH2:1]([CH2:4][NH:5][C:6]([CH3:10])([CH3:9])[CH2:7][NH2:8])[CH:2]=[CH2:3].[Cl:11][C:12]1[CH:13]=[C:14]([CH:18]=[CH:19][C:20]=1[Cl:21])[C:15](Cl)=[O:16]>C1C=CC=CC=1.C(OCC)(=O)C>[Cl:11][C:12]1[CH:13]=[C:14]([CH:18]=[CH:19][C:20]=1[Cl:21])[C:15]([NH:8][CH2:7][C:6]([NH:5][CH2:4][CH2:1][CH:2]=[CH2:3])([CH3:10])[CH3:9])=[O:16]
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참가 물질

5

반응물 2

HCID 76403Benzoyl chloride, 3,4-dichloro-HCID 55284641HCID 55284641, 화합물

생성물 1

HCID 21409887HCID 21409887, 화합물

시약·촉매·용매 2

HCID 241Benzene용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 2-allylmethylamino-2-methylpropylamine (1.3 g.,) and 3,4-dichlorobenzoyl chloride (3.15 g.,) was heated under reflux in dry benzene (150 ml.) for 1 hrs. The cooled mixture was washed with dilute sodium hydroxide solution (2 × 30 ml.), water (2 × 30 ml.), dried (MgSO4) and the solvent was removed in vacuo to give a yellow oil (3.9 g.). The oil was passed through a column of alumina 40 × 2.5 cm. using ethyl acetate as an eluent to give 3,4-dichloro-N-(2-allylmethylamino-2-methylpropyl)-benzamide as a pale yellow liquid (2.25 g., 71%).

후처리

  1. temperaturewas heated
  2. washThe cooled mixture was washed with dilute sodium hydroxide solution (2 × 30 ml.), water (2 × 30 ml.)
  3. dry with materialdried (MgSO4)
  4. customthe solvent was removed in vacuo
  5. customto give a yellow oil (3.9 g.)

출처 및 근거

ORD 기록
ord-f5fac60df1174815b1dc8098470d04b7
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04049663

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