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3,4-Diethoxybenzaldehyde → Methyl 3-(3,4-diethoxyphenyl)prop-2-enoate

HRID 987863
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인쇄 미리보기

반응식

HRID 987863 반응식
C1(P(=C=[CH:21][C:22]([O:24][CH3:25])=[O:23])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:26]([O:28][C:29]1[CH:30]=[C:31]([CH:34]=[CH:35][C:36]=1[O:37][CH2:38][CH3:39])[CH:32]=O)[CH3:27]>C1(C)C=CC=CC=1>[CH2:26]([O:28][C:29]1[CH:30]=[C:31](/[CH:32]=[CH:21]/[C:22]([O:24][CH3:25])=[O:23])[CH:34]=[CH:35][C:36]=1[O:37][CH2:38][CH3:39])[CH3:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 748473,4-DiethoxybenzaldehydeHCID 12530579HCID 12530579, 화합물

생성물 1

HCID 22987080Methyl 3-(3,4-diethoxyphenyl)prop-2-enoate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

1.81 g (5.40 mmol) of methyl (triphenylphosphoranylidene)acrylate are added, at room temperature, to a solution of 1.0 g (5.15 mmol) of 3,4-diethoxybenzaldehyde and 10 ml of toluene. The reaction is then allowed to proceed for 1 hour at room temperature, the reaction suspension is clarified by filtration over a silica gel bed and the filtrate is evaporated down. Chromatography of the residue over silica gel using toluene/ethyl acetate gives methyl 3(E)-(3,4-diethoxyphenyl)acrylate.

후처리

  1. filtrationthe reaction suspension is clarified by filtration over a silica gel bed
  2. customthe filtrate is evaporated down

출처 및 근거

ORD 기록
ord-81299d9006da4fc292171c3448b13661
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06632909B2

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