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Acetic Anhydride → 7-Methoxyisochroman-1,3-dione

HRID 1182922
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HRID 1182922 반응식
[O:1]([C:3]1[CH:4]=[C:5]([C:13]([OH:15])=[O:14])[C:6](=[CH:11][CH:12]=1)[CH2:7][C:8]([OH:10])=O)[CH3:2].C(OC(=O)C)(=O)C>C1(C)C=CC=CC=1>[O:1]([C:3]1[CH:4]=[C:5]2[C:13](=[O:14])[O:15][C:8](=[O:10])[CH2:7][C:6]2=[CH:11][CH:12]=1)[CH3:2]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 23054232-(carboxymethyl)-5-methoxybenzoic acid

생성물 1

HCID 121967027-Methoxyisochroman-1,3-dione수율 110.1%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

1.1 g (5.2 mmol) of 4-methoxylhomophthalic acid (IIb) was dissolved in 20 ml toluene, and 0.7 ml (7.9 mmol) of acetic anhydride was added. The mixture was heated to the reflux temperature and reacted for 0.5 h. Then, the reaction mixture was cooled to the room temperature and concentrated to dry in a reduced pressure to obtain 1.1 g of a pale yellow solid with the yield of 100%. m.p. 142-143° C.

후처리

  1. temperatureThe mixture was heated to the reflux temperature
  2. customreacted for 0.5 h
  3. concentrationconcentrated
  4. customto dry in a reduced pressure

출처 및 근거

ORD 기록
ord-0e854e3c0041495d83017d510ade7a4a
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664238B2

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