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2-Dimethylaminopyridine → 2,4-Dichloro-6-methyloxybenzoyl chloride

HRID 1073481
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HRID 1073481 반응식
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]([O:12][CH3:13])[C:3]=1[C:4](O)=[O:5].CN(C1C=CC=CN=1)C.S(Cl)([Cl:25])=O>C(Cl)Cl>[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]([O:12][CH3:13])[C:3]=1[C:4]([Cl:25])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 218852-DimethylaminopyridineHCID 24386Thionyl ChlorideHCID 135533172,4-Dichloro-6-methoxybenzoic acid

생성물 1

HCID 137948482,4-Dichloro-6-methyloxybenzoyl chloride수율 55%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

26.0 g. (0.117 mol) 2,4-Dichloro-6-methoxybenzoic acid were dissolved in 50 ml. anhydrous methylene chloride and, after the addition of 0.1 g. dimethylaminopyridine, 50 ml. thionyl chloride were added dropwise thereto at ambient temperature. After stirring for 15 hours, the reaction mixture was evaporated and the residue distilled. Yield: 55% of theory; b.p. 118-124° C./0.1 mm.Hg.

후처리

  1. customat ambient temperature
  2. customthe reaction mixture was evaporated
  3. distillationthe residue distilled

출처 및 근거

ORD 기록
ord-54c91ab192824b9c8107ede9611926c7
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04970077

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