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Thionyl Chloride → 2,4-Dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoyl chloride

HRID 659932
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인쇄 미리보기

반응식

HRID 659932 반응식
[Cl:1][C:2]1[C:10]([O:11][CH2:12][CH2:13][N:14]2[CH:18]=[N:17][N:16]=[N:15]2)=[C:9]([Cl:19])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:22])=O>ClCCCl.CN(C=O)C>[Cl:1][C:2]1[C:10]([O:11][CH2:12][CH2:13][N:14]2[CH:18]=[N:17][N:16]=[N:15]2)=[C:9]([Cl:19])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:22])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 574372702,4-Dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoic acid

생성물 1

HCID 574372552,4-Dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoyl chloride수율 100.4%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 111,2-Dichloroethane용매

실험 절차

2,4-dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoic acid (0.46 g) and thionyl chloride (0.36 g) were added in 1,2-dichloroethane (10 ml), two drops of DMF were added and the mixture was refluxed by heating for 3 hours. After cooling, the solvent was distilled off to obtain the desired 2,4-dichloro-3-[2-(1H-tetrazol-1-yl)ethoxy]benzoyl chloride (0.49 g).

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureby heating for 3 hours
  3. temperatureAfter cooling
  4. distillationthe solvent was distilled off

출처 및 근거

ORD 기록
ord-59b7f4b5e21b46cea63560e22aade3c5
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084398B2

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