Acetic Anhydride → 3-Acetoxy-5-benzyloxybenzoic acid

HRID 1713299노트

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HRID 1713299 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:15]=[C:16]([OH:18])[CH:17]=1)[C:12]([OH:14])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19](OC(=O)C)(=[O:21])[CH3:20]>C(O)(=O)C>[C:19]([O:18][C:16]1[CH:15]=[C:11]([CH:10]=[C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:17]=1)[C:12]([OH:14])=[O:13])(=[O:21])[CH3:20]

참가 물질

4

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온도
120 °C

실험 절차

3-Benzyloxy-5-hydroxybenzoic acid (2.16 g) and acetic anhydride (15 mL) were suspended in acetic acid (15 mL), and the resulting mixture was stirred at 120° C. for 24 hours. The reaction mixture was concentrated under reduced pressure and the residue obtained was purified by column chromatography on silica gel (eluent: ethyl acetate/hexane=1/1 to 1/0) to give the title compound (1.74 g).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe residue obtained
  3. customwas purified by column chromatography on silica gel (eluent: ethyl acetate/hexane=1/1 to 1/0)

출처 및 근거

ORD 기록
ord-2b059118e70d4af8a7e9ef26f4064e66
출처 데이터셋
uspto-grants-2010_09
특허 번호
US07795236B2

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