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Alpha-Methylstyrene → Cumyl dithiobenzoate

HRID 1297477
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인쇄 미리보기

반응식

HRID 1297477 반응식
[C:1]([SH:9])(=[S:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:10][C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[CH2:12]>C(Cl)(Cl)(Cl)Cl>[C:1]([S:9][C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([CH3:12])[CH3:10])(=[S:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7407Alpha-MethylstyreneHCID 67141Benzenecarbodithioic acid

생성물 1

HCID 11065602Cumyl dithiobenzoate수율 32.6%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

반응 조건

온도
70 °C

실험 절차

A mixture of dithiobenzoic acid (10.59 g), a-methylstyrene (10 g) and carbon tetrachloride (40 mL) was heated at 70° C. for 4 hours. The resultant mixture was reduced to a crude oil which was purified by column chromatography (aluminium oxide (activity III), n-hexane eluent) to give 2-phenylprop-2-yl dithiobenzoate (5) (6.1 g, 32.6% yield) as a dark purple oil. 1H-nmr (CDCl3) d(ppm): 2.03 (s, 6H); 7.20-7.60 (m, 8H) and 7.86 (m, 2H).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customwas purified by column chromatography (aluminium oxide (activity III), n-hexane eluent)

출처 및 근거

ORD 기록
ord-3cd00bcf174e4831bfb6f9b86e8987ab
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07250479B2

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