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Benzyl Bromide → HCID 18923724, 화합물

HRID 1290164
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HRID 1290164 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([Cl:10])[CH:9]=1)[NH:5][CH3:6].[CH2:11](Br)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>C(#N)C>[CH2:11]([N:5]([CH3:6])[C:4]1[CH:3]=[C:2]([Cl:1])[CH:9]=[C:8]([Cl:10])[CH:7]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 8471TriethylamineHCID 123777573,5-Dichloro-N-methylaniline

생성물 1

HCID 18923724HCID 18923724, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

The mixture of 3,5-dichloro-N-methylaniline (345 mg) and excess amount of benzyl bromide and triethylamine in acetonitrile (7 ml) was refluxed for 4 hours. The reaction mixture was separated with ethyl acetate and water, and the organic layer was washed with water, dried and concentrated in vacuo to give N-benzyl-3,5-dichloro-N-methylaniline (532 mg).

후처리

  1. temperaturewas refluxed for 4 hours
  2. customThe reaction mixture was separated with ethyl acetate and water
  3. washthe organic layer was washed with water
  4. customdried
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b35469c020ae486fa123b4406c5b2a24
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750699

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