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Triphenylphosphine → Triphenyl(3-pyridylmethyl)phosphonium chloride

HRID 496066
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인쇄 미리보기

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HRID 496066 반응식
[C:1]1([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:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[N:21]1[CH:26]=[CH:25][CH:24]=[C:23]([CH2:27][Cl:28])[CH:22]=1>CN(C)C=O>[Cl-:28].[C:14]1([P+:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:27][C:23]2[CH:22]=[N:21][CH:26]=[CH:25][CH:24]=2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 233943-(Chloromethyl)pyridine hydrochloride

생성물 1

HCID 22325077Triphenyl(3-pyridylmethyl)phosphonium chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
5 °C

실험 절차

13.1 g of triphenyphosphine are added to a solution of 8.2 g of 3-picolyl chloride hydrochloride in 120 ml of dimethylformamide. After stirring for 5 minutes, the mixture is heated at reflux for 30 minutes in a microwave apparatus and then cooled to 5° C. The crystals obtained are filtered off, rinsed with dimethylformamide and then with ether, and dried under reduced pressure, allowing the expected product to be isolated.

후처리

  1. temperaturethe mixture is heated
  2. temperatureat reflux for 30 minutes in a microwave apparatus
  3. customThe crystals obtained
  4. filtrationare filtered off
  5. washrinsed with dimethylformamide
  6. dry with materialwith ether, and dried under reduced pressure
  7. customto be isolated

출처 및 근거

ORD 기록
ord-cdcd86a29f9a48d5935f932b22154baa
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943184B2

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