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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 10899796, 화합물

HRID 1410548
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HRID 1410548 반응식
[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4]Cl.O.Cl.[NH:12]1[CH2:17][CH2:16][C:15](=[O:18])[CH2:14][CH2:13]1.C(N(CC)CC)C>ClCCl>[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][N:12]1[CH2:17][CH2:16][C:15](=[O:18])[CH2:14][CH2:13]1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 9580Benzene, 1-(chloromethyl)-2-fluoro-HCID 2723901Piperonylamine

생성물 1

HCID 10899796HCID 10899796, 화합물수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

64.00 g (0.443 mol) of o-fluorobenzylchloride was weighed, to which 250 mL of dichloromethane was added. 62.40 g (0.406 mol) of 4-piperidone hydrochloride monohydrate was added under stirring, and then 91.00 g (0.899 mol) of triethylamine was added dropwise under cold water cooling and stirring. The reaction was stirred at room temperature for 4.5 h, and then stirred under reflux and reacted overnight. On the next day, the reaction was cooled, filtered to remove solid, washed in sequence with dichloromethane and ethyl ether, combined, washed with water and dried, and the solvent was recovered to obtain 68.95 g crude product (82.00%), which was used directly in the next reaction.

후처리

  1. additionwas added
  2. stirringstirring
  3. stirringThe reaction was stirred at room temperature for 4.5 h
  4. stirringstirred
  5. temperatureunder reflux
  6. customreacted overnight
  7. temperatureOn the next day, the reaction was cooled
  8. filtrationfiltered
  9. customto remove solid
  10. washwashed in sequence with dichloromethane and ethyl ether
  11. washwashed with water
  12. customdried
  13. customthe solvent was recovered

출처 및 근거

ORD 기록
ord-f98bbc9cac0f44a7aceebe3694228a7f
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921563B2

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