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Thionyl Chloride → 1-tert-Butyl-4-(chloromethyl)-2-isopropylbenzene

HRID 1675256
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인쇄 미리보기

반응식

HRID 1675256 반응식
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11]O)=[CH:7][C:6]=1[CH:13]([CH3:15])[CH3:14])([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:18])=O>C(Cl)Cl>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][Cl:18])=[CH:7][C:6]=1[CH:13]([CH3:15])[CH3:14])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 59300613(4-tert-Butyl-3-isopropylphenyl)methanol

생성물 1

HCID 593006801-tert-Butyl-4-(chloromethyl)-2-isopropylbenzene수율 96.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Alcohol 26.4 (77.0 mg, 0.37 mmol) was dissolved in anhydrous DCM (5.0 mL). Thionyl chloride (0.041 mL, 0.56 mmol) was added dropwise to the above solution. The resulting mixture was stirred at room temperature for 24 hours. The organic solvent was then removed under vacuo to give a white solid (80 mg). The crude product (26.5) was used in the next step without further purification.

후처리

  1. customThe organic solvent was then removed under vacuo

출처 및 근거

ORD 기록
ord-3550e94759c642fd906a6f7dc7c0103e
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003648B2

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