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2-Bromo-1-(4-fluorophenyl)ethan-1-one → N-(4-fluorobenzoylmethyl)-2,2-dimethyl-1,2,3,4-tetrahydroquinoline

HRID 373581
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인쇄 미리보기

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HRID 373581 반응식
[CH3:1][C:2]1([CH3:12])[CH2:11][CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[NH:3]1.Br[CH2:14][C:15]([C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)=[O:16]>CN(C)C=O>[F:23][C:20]1[CH:21]=[CH:22][C:17]([C:15]([CH2:14][N:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[CH2:10][CH2:11][C:2]2([CH3:12])[CH3:1])=[O:16])=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 967492-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 134958062,2-Dimethyl-1,2,3,4-tetrahydroquinoline

생성물 1

HCID 19810696N-(4-fluorobenzoylmethyl)-2,2-dimethyl-1,2,3,4-tetrahydroquinoline수율 85.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A stirred mixture of 2,2-dimethyl-1,2,3,4-tetrahydroquinoline (4.69 g) and 2-bromo-4'-fluoroacetophenone (3.17 g) in dry N,N-dimethylformamide (6 ml) was heated at 70°-80° C. for 5 hours under nitrogen. The reaction mixture was poured was triturated with diethyl ether to give pale yellow crystals. The crystals were collected and washed with methanol to give N-(4-fluorobenzoylmethyl)-2,2-dimethyl-1,2,3,4-tetrahydroquinoline (3.7 g).

후처리

  1. temperaturewas heated at 70°-80° C. for 5 hours under nitrogen
  2. additionThe reaction mixture was poured
  3. customwas triturated with diethyl ether
  4. customto give pale yellow crystals
  5. customThe crystals were collected
  6. washwashed with methanol

출처 및 근거

ORD 기록
ord-ec87b701324f4fecb7f2ebe054e1a1cb
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05164400

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