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Thionyl Chloride → 4-Iodo-2-methoxybenzoyl chloride

HRID 1708375
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HRID 1708375 반응식
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1.S(Cl)([Cl:15])=O>>[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([Cl:15])=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1
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참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 134507564-Iodo-2-methoxybenzoic acid

생성물 1

HCID 189587634-Iodo-2-methoxybenzoyl chloride

실험 절차

A mixture of 4-iodo-2-methoxybenzoic acid (750 mg) and thionyl chloride (7 ml) was stirred at reflux for 15min and then evaporated to give 4-iodo-2-methoxybenzoyl chloride. A solution of Intermediate 6 (629 mg) in THF (30 ml) was treated with a solution of sodium hydroxide (227 mg) in water (10 ml), followed by the 4-iodo-2-methoxybenzoyl chloride, and the mixture stirred at 23° under nitrogen for 24 h. 5M-Hydrochloric acid (1.5 ml) was added, followed by aqueous saturated sodium bicarbonate (10 ml), and the mixture evaporated. The residue was treated with water (50 ml), extracted with ethyl acetate (10×100 ml), and the combined, dried organic extracts were evaporated. The residue was adsorbed from hot ethanol (ca. 40 ml) onto silica gel (Merck 7734, 10 ml), and purified by FCC eluting with System A (945:50:5) to give a solid (780 mg). Crystallisation from ethanol (10 ml) gave the impure title compound, a portion of which (102 mg) was recrystallised from ethanol to give the pure title compound as fine white crystals (37 mg), m.p. 168°-170°.

후처리

  1. temperatureat reflux for 15min
  2. customevaporated

출처 및 근거

ORD 기록
ord-1b0dfefec2bf42e291fbc0a7a60c8d2b
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05358948

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