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Ethyl 3,3-bis(4-fluorophenyl)acrylate → Ethyl 3,3-bis(4-fluorophenyl)propanoate

HRID 2190300
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인쇄 미리보기

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HRID 2190300 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=2)=[CH:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1.[H][H]>[Pd].CCO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([C:15]2[CH:16]=[CH:17][C:18]([F:21])=[CH:19][CH:20]=2)[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21908058Ethyl 3,3-bis(4-fluorophenyl)acrylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 23522917Ethyl 3,3-bis(4-fluorophenyl)propanoate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a mixture of ethyl 3,3-bis(4-fluorophenyl)acrylate, prepared in the previous step, and palladium (10% weight on carbon, 2.68 g, 25.2 mmol) under a nitrogen atmosphere was added EtOH (100 mL). The nitrogen atmosphere was replaced by hydrogen from a double balloon and the reaction mixture was stirred at room temperature. After 16 h, the reaction mixture was filtered through a pad of Celite and concentrated to give ethyl 3,3-bis(4-fluorophenyl)propanoate which was used in the next step without further purification.

후처리

  1. filtrationthe reaction mixture was filtered through a pad of Celite
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c754dd11be5d4d19a08c9163c9cc979f
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324396B2

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