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Acetic Anhydride → 3-Allyl-4-acetoxy-cinnamic acid

HRID 259610
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인쇄 미리보기

반응식

HRID 259610 반응식
[CH2:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[OH:15])[CH:7]=[CH:8][C:9]([OH:11])=[O:10])[CH:2]=[CH2:3].[C:16](OC(=O)C)(=[O:18])[CH3:17]>[OH-].[Na+]>[CH2:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[O:15][C:16](=[O:18])[CH3:17])[CH:7]=[CH:8][C:9]([OH:11])=[O:10])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 540628753-Allyl-4-hydroxy-cinnamic acid

생성물 1

HCID 538871623-Allyl-4-acetoxy-cinnamic acid

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

118 g (0.058 mol) of 3-allyl-4-hydroxy-cinnamic acid are dissolved in 580 ml of 2 N sodium hydroxide solution, 800 g of ice are added and 120 g (1.16 mols) of acetic anhydride are introduced dropwise over the course of 15 minutes at 0°-5° C., whilst stirring. The crystals which have precipitated are then separated off, suction-dried and recrystallised from ethyl acetate. 3-Allyl-4-acetoxy-cinnamic acid of melting point 143°-144° C. is thus obtained.

후처리

  1. customThe crystals which have precipitated
  2. customare then separated off
  3. customsuction-dried
  4. customrecrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-d8b78ea90688407799f4a483bbba9d58
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04038414

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