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Benzaldehyde → Z-2-(4-fluorophenyl)-3-phenylpropenal

HRID 653629
노트
인쇄 미리보기

반응식

HRID 653629 반응식
[OH-].[Na+].[CH:3](=O)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[F:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH:19]=[O:20])=[CH:14][CH:13]=1>O.CO>[F:11][C:12]1[CH:17]=[CH:16][C:15](/[C:18](=[CH:3]/[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)/[CH:19]=[O:20])=[CH:14][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 240BenzaldehydeHCID 14798Sodium HydroxideHCID 111263222-(4-Fluorophenyl)acetaldehyde

생성물 1

HCID 15096607Z-2-(4-fluorophenyl)-3-phenylpropenal

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

반응 조건

온도
10 °C

실험 절차

4.2 g of sodium hydroxide in 30 ml of water are added to a solution of 26.5 g of benzaldehyde in 300 ml of methanol. The reaction mixture is cooled to 10° C., and 36 g of 4-fluorophenylacetaldehyde are rapidly added, during which the solution rises to 30°-40° C. The reaction solution is stirred at 40° C. for 10 hours and then cooled and the crystals which have separated out are filtered off with suction. 31.6 g (56%) of E/Z-2-(4-fluorophenyl)-3-phenylpropenal of melting point 87°-94° C. are obtained.

후처리

  1. customrises to 30°-40° C
  2. temperaturecooled
  3. customthe crystals which have separated out
  4. filtrationare filtered off with suction

출처 및 근거

ORD 기록
ord-771f3ddb1bbe4fbca791b3413d88484b
출처 데이터셋
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05128357

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