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Triethyl phosphite → 2-Bromo-7-chloro-3-diethylphosphonomethyl-6-methylquinoline

HRID 726648
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HRID 726648 반응식
[Br:1][C:2]1[C:11]([CH2:12]Br)=[CH:10][C:9]2[C:4](=[CH:5][C:6]([Cl:15])=[C:7]([CH3:14])[CH:8]=2)[N:3]=1.[CH2:16]([O:18][P:19]([O:23]CC)[O:20][CH2:21][CH3:22])[CH3:17]>C1(C)C=CC=CC=1>[Br:1][C:2]1[C:11]([CH2:12][P:19]([O:20][CH2:21][CH3:22])([O:18][CH2:16][CH3:17])=[O:23])=[CH:10][C:9]2[C:4](=[CH:5][C:6]([Cl:15])=[C:7]([CH3:14])[CH:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31215Triethyl phosphiteHCID 227450662-Bromo-3-bromomethyl-7-chloro-6-methylquinoline

생성물 1

HCID 542836542-Bromo-7-chloro-3-diethylphosphonomethyl-6-methylquinoline

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 2-bromo-3-bromomethyl-7-chloro-6-methylquinoline (4.2 g, 12 mmol), toluene (50 ml) and triethylphosphite (4.2 ml) was refluxed for 20 h. After cooling the solution was concentrated in vacuum and the product precipitated by the addition of hexane. The crystals were filtered off, washed with hexane and dried in vacuo to give 4.5 g of 2-bromo-7-chloro-3-diethylphosphonomethyl-6-methylquinoline.

후처리

  1. temperaturewas refluxed for 20 h
  2. temperatureAfter cooling the solution
  3. concentrationwas concentrated in vacuum
  4. customthe product precipitated by the addition of hexane
  5. filtrationThe crystals were filtered off
  6. washwashed with hexane
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-517e95cd09e240ff9acb26379f36ec3c
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05710139

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