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Benzaldehyde → Ethyl cinnamoylacetate

HRID 34484
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인쇄 미리보기

반응식

HRID 34484 반응식
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(N(CC)CC)C>C(Cl)(Cl)(Cl)Cl.O1CCCC1.[Ti](Cl)(Cl)(Cl)Cl>[O:4]=[C:3]([CH:5]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:2][C:1]([O:7][CH2:8][CH3:9])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 240BenzaldehydeHCID 8471TriethylamineHCID 8868Ethyl Acetoacetate

생성물 1

HCID 54004396Ethyl cinnamoylacetate

시약·촉매·용매 3

HCID 24193Titanium Tetrachloride촉매HCID 5943Carbon Tetrachloride용매
HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

A solution of 0.020 moles of titanium tetrachloride in 15 ml of carbon tetrachloride was added over a period of 10 minutes to a cold (5°) solution of 0.015 moles of ethyl acetoacetate and 0.015 moles of benzaldehyde in 60 ml of tetrahydrofuran. After the mixture was stirred for 1.5 hours, a solution of 0.060 mole of triethylamine in 15 ml of tetrahydrofuran was added dropwise. The reaction mixture was then stirred for 20 hours, after which the title compound was isolated by the extraction and chromatography methods described in Example 1. The material prepared by this procedure was identical to that prepared by the method of Example 1, as indicated by the reverse phase chromatographic method described in Example 2.

후처리

  1. stirringThe reaction mixture was then stirred for 20 hours

출처 및 근거

ORD 기록
ord-7d7bafc6893e4fa1b0645219b53a09c3
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04761503

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