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Thionyl Chloride → 4-Isopropoxy-3-methoxybenzoyl chloride

HRID 1478425
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HRID 1478425 반응식
[CH:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](O)=[O:10])=[CH:7][C:6]=1[O:14][CH3:15])([CH3:3])[CH3:2].S(Cl)([Cl:18])=O>ClCCl>[CH:1]([O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([Cl:18])=[O:10])=[CH:7][C:6]=1[O:14][CH3:15])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 24386Thionyl Chloride2회HCID 20639154-Isopropoxy-3-methoxybenzoic acid

생성물 1

HCID 467796444-Isopropoxy-3-methoxybenzoyl chloride수율 101.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
30 °C

실험 절차

To a stirring solution of 4-isopropoxy-3-methoxy-benzoic acid (40.0 g, 190.3 mmol) in anhydrous dichloromethane (400 mL) at room temperature was slowly added thionyl chloride (27.8 mL, 381 mmol). The reaction was then transferred from a room temperature water bath to an oil bath that was then warmed to 30° C. The solution was allowed to stir overnight at 30° C. The reaction mixture was allowed to cool to room temperature prior to the addition of additional thionyl chloride (10.0 mL, 137 mmol). The reaction was allowed to stir at 40° C. for 3 hours. After completion, the reaction mixture was concentrated under reduced pressure, azeotrophing with toluene to provide 4-isopropoxy-3-methoxy-benzoyl chloride (44.3 g) as a yellow oil. The product was used in the next step without further purification.

후처리

  1. customat room temperature
  2. customwas then transferred from a room temperature
  3. temperatureto cool to room temperature
  4. stirringto stir at 40° C. for 3 hours
  5. concentrationAfter completion, the reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-bdaa423ee2cc44c78c5b60acb607e06a
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09403839B2

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