2,4,5-Trimethoxybenzoic acid → 2,4,5-Trimethoxybenzoyl chloride

HRID 1106445

반응식

HRID 1106445 반응식
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([O:12][CH3:13])[C:9]([O:14][CH3:15])=[CH:8][C:4]=1[C:5](O)=[O:6].S(Cl)([Cl:18])=O>C1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([O:12][CH3:13])[C:9]([O:14][CH3:15])=[CH:8][C:4]=1[C:5]([Cl:18])=[O:6]

참가 물질

4

반응물 2

HCID 102762,4,5-Trimethoxybenzoic acidHCID 24386Thionyl Chloride

생성물 1

HCID 27608092,4,5-Trimethoxybenzoyl chloride수율 89.7%

시약·촉매·용매 1

HCID 241Benzene용매

반응 조건

온도
70 °C

실험 절차

To a suspension of 2,4,5-trimethoxybenzoic acid (2.12 g, 10 mmol) in dry 10 mL benzene was added thionyl chloride (4.4 mL, 60 mmol). The reaction mixture was stirred at 70° C. for 5 hr. The solvent was evaporated in vacuo. The residue was washed with hexane to give 2.07 g of the title compound which was used for the next step without further purification. 1H NMR (CDCl3) δ: 7.65 (1 H, s), 6.50 (1 H, s), 4.05 (3 H, s), 3.97 (3 H, s), 3.86 (3 H, s).

후처리

  1. customThe solvent was evaporated in vacuo
  2. washThe residue was washed with hexane

출처 및 근거

ORD 기록
ord-6c4662da3acb424caf91f7c4bb1cc266
출처 데이터셋
uspto-grants-2000_05
특허 번호
US06057315

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