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Thionyl Chloride → 2-(3,4,5-Trimethoxyphenyl)benzyl chloride

HRID 1634868
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HRID 1634868 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=2[CH2:15]O)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].S(Cl)([Cl:23])=O>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=2[CH2:15][Cl:23])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 213388232-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

생성물 1

HCID 120163292-(3,4,5-Trimethoxyphenyl)benzyl chloride

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2-(3,4,5-Trimethoxyphenyl)benzyl alcohol (630 mg) was dissolved in chloroform (10 mL), and to the solution thionyl chloride (0.153 mL) was added at 0° C. After 30 minutes, the mixture was warmed to room temperature and stirred for 4 hours. The reaction mixture was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was then recrystallized from chloroform-hexane to obtain the title compound.

후처리

  1. washThe reaction mixture was washed with water and saturated brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was then recrystallized from chloroform-hexane

출처 및 근거

ORD 기록
ord-3594760b0a684fcca052647f78d4465c
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06509329B1

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