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Methyl 2-(bromomethyl)-3-phenylacrylate → (E)-2-Formyloxymethyl-3-phenylacrylic acid methyl ester

HRID 1071578
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인쇄 미리보기

반응식

HRID 1071578 반응식
[CH:1]([O-:3])=[O:2].C([NH+](CC)CC)C.[CH3:11][O:12][C:13](=[O:24])/[C:14](/[CH2:22]Br)=[CH:15]/[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(#N)C>[CH3:11][O:12][C:13](=[O:24])/[C:14](/[CH2:22][O:3][CH:1]=[O:2])=[CH:15]/[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5904127Methyl 2-(bromomethyl)-3-phenylacrylateHCID 10219518Triethylazanium;formate

생성물 1

HCID 86759761(E)-2-Formyloxymethyl-3-phenylacrylic acid methyl ester

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a stirred solution of triethylammonium formate (1.87 g) in acetonitrile (4 ml) was added (Z)-2-bromomethyl-3-phenylacrylic acid methyl ester (1.30 g) and the mixture heated at reflux for 2 hours. The reaction was cooled and extracted into diethyl ether (3×10 ml). The combined organics were dried (MgSO4) and concentrated under reduced pressure to afford the title compound as a crude oil.

후처리

  1. temperaturethe mixture heated
  2. temperatureat reflux for 2 hours
  3. temperatureThe reaction was cooled
  4. extractionextracted into diethyl ether (3×10 ml)
  5. dry with materialThe combined organics were dried (MgSO4)
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a7d56f59ddeb45fbaac69457384e656a
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06906085B2

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