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4-Nitrobenzyl chloride → 4-Nitrobenzyltriphenylphosphonium chloride

HRID 26402
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인쇄 미리보기

반응식

HRID 26402 반응식
[CH:1]1[CH:6]=[CH:5][C:4]([P:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:3][CH:2]=1.[N+:20]([C:23]1[CH:30]=[CH:29][C:26]([CH2:27][Cl:28])=[CH:25][CH:24]=1)([O-:22])=[O:21]>>[Cl-:28].[N+:20]([C:23]1[CH:30]=[CH:29][C:26]([CH2:27][P+:7]([C:4]2[CH:3]=[CH:2][CH:1]=[CH:6][CH:5]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:25][CH:24]=1)([O-:22])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 74824-Nitrobenzyl chlorideHCID 11776Triphenylphosphine

생성물 1

HCID 120003154-Nitrobenzyltriphenylphosphonium chloride

실험 절차

A solution of 26.3 g (0.10 moles) of triphenylphosphide and 17.2 g (0.10 moles) of p-nitrobenzyl chloride in 50 ml of benezene is refluxed for 2 hours. After cooling the solid is collected and washed with benzene. Crystallization from carbon tetrachloride petroleum ether gives colorless crystals, m.p. 278°-280° C.

후처리

  1. temperatureAfter cooling the solid
  2. customis collected
  3. washwashed with benzene
  4. customCrystallization from carbon tetrachloride petroleum ether
  5. customgives colorless crystals, m.p. 278°-280° C.

출처 및 근거

ORD 기록
ord-6e5bd4e07c044528b4ceaa1ba598509a
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04150105

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