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3-Phenylprop-2-En-1-Ol → Ethyl 2-acetyl-3-phenyl-4-pentenoate

HRID 1982615
노트
인쇄 미리보기

반응식

HRID 1982615 반응식
[CH2:1](O)[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C([O:13]/[C:14](/[CH3:21])=[CH:15]\[C:16]([O:18][CH2:19][CH3:20])=[O:17])C>P(=O)(O)(O)O.C(O)C>[C:14]([CH:15]([CH:3]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[CH:2]=[CH2:1])[C:16]([O:18][CH2:19][CH3:20])=[O:17])(=[O:13])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 3083-Phenylprop-2-En-1-OlHCID 5904488Ethyl 3-ethoxy-2-butenoate

생성물 1

HCID 13646832Ethyl 2-acetyl-3-phenyl-4-pentenoate수율 85.4%

시약·촉매·용매 2

HCID 1004Phosphoric Acid촉매HCID 702Ethanol용매

반응 조건

온도
150 °C

실험 절차

The starting material was prepared as follows. To a mixture of 4.02 g of cinnamyl alcohol and 6.6 g of ethyl β-ethoxycrotonate was added 10 mg of phosphoric acid. The resulting mixture was heated to a temperature of 150° C. over a period of about 40 minutes and then heated at 150° C. for 4 hours with stirring while the ethanol formed during the reaction was distilled off. Thereafter, the reaction mixture was distilled to give 6.3 g (81% yield) of ethyl 2-acetyl-3-phenyl-4-pentenoate, boiling point 170°-174° C./20 mmHg.

후처리

  1. customThe starting material was prepared
  2. temperatureheated at 150° C. for 4 hours
  3. customformed during the reaction
  4. distillationwas distilled off
  5. distillationThereafter, the reaction mixture was distilled

출처 및 근거

ORD 기록
ord-fdf5bf3eceda48aaad09f8d8f0780593
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596887

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