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Allyl bromide → N-[2-n-Pentyl-3-(2,4-dichlorophenyl)-prop-2-en-1-yl]-N-allyl-pyrrolidinium bromide

HRID 2418269
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HRID 2418269 반응식
[CH2:1]([C:6](=[CH:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=1[Cl:21])[CH2:7][N:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH2:2][CH2:3][CH2:4][CH3:5].[CH2:22]([Br:25])[CH:23]=[CH2:24]>C(O)(=O)C>[Br-:25].[CH2:1]([C:6](=[CH:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=1[Cl:21])[CH2:7][N+:8]1([CH2:24][CH:23]=[CH2:22])[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH2:2][CH2:3][CH2:4][CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7841Allyl bromideHCID 54067199HCID 54067199, 화합물

생성물 1

HCID 86739637N-[2-n-Pentyl-3-(2,4-dichlorophenyl)-prop-2-en-1-yl]-N-allyl-pyrrolidinium bromide수율 53.8%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

19 g of (IV) and 14.5 g of allyl bromide in 200 ml of glacial acetic acid were refluxed for 5 hours, the mixture was cooled, and the liquid product which separated out was triturated with ethyl acetate. The product which crystallized out was filtered off under suction, washed with ethyl acetate and dried under reduced pressure. 14 g of (V) of melting point 109° C. were obtained (compound No. 3a).

후처리

  1. temperaturethe mixture was cooled
  2. customthe liquid product which separated out
  3. customwas triturated with ethyl acetate
  4. customThe product which crystallized out
  5. filtrationwas filtered off under suction
  6. washwashed with ethyl acetate
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-7965937573014f8fbff04de36f2e1b07
출처 데이터셋
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04472412

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