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Salicylic Acid → Aspirin

HRID 1984998
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인쇄 미리보기

반응식

HRID 1984998 반응식
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11](OC(=O)C)(=[O:13])[CH3:12]>COC1C=CC(C2OC(C3C=CC(OC)=C(OC)C=3)CCC2)=CC=1OC>[C:11]([O:4][C:3]1[C:2](=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:1]([OH:10])=[O:9])(=[O:13])[CH3:12]
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참가 물질

4

반응물 2

HCID 338Salicylic Acid2회HCID 7918Acetic Anhydride

생성물 1

HCID 2244Aspirin

시약·촉매·용매 1

HCID 1325512,6-Bis(3,4-dimethoxyphenyl)oxane촉매

반응 조건

온도
100 °C

실험 절차

0.0072 moles of salicylic acid and 0.029 moles acetic anhydride (molar ratio=1:4) were taken in a 20 ml reaction vessel of reaction station. Nano-crystalline sulfated zirconia catalyst (SZ-1), activated at 450° C. in static air with salicylic acid to catalyst weight ratio 10:1, was added and the mixture was heated at 100° C. for 30 minutes. The reaction mixture was filtered to separate the catalyst. The acetyl salicylic acid was crystallized from the reaction mixture. The crude yield of acetyl salicylic acid was 73%. It was further re-crystallized with ethanol-water to obtain pure crystals of acetyl salicylic acid.

후처리

  1. additionwas added
  2. filtrationThe reaction mixture was filtered
  3. customto separate the catalyst
  4. customThe acetyl salicylic acid was crystallized from the reaction mixture
  5. customIt was further re-crystallized with ethanol-water

출처 및 근거

ORD 기록
ord-3445184ce49944a996455d69ba409fb5
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544831B2

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