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Vanillin → 3-(4-Hydroxy-3-methoxyphenyl)-1-phenyl-2-propen-1-one

HRID 716608
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HRID 716608 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[OH:11])[CH:6]=O.[C:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:14])[CH3:13]>C(O)(=O)C>[OH:11][C:10]1[CH:9]=[CH:8][C:5]([CH:6]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:14])=[CH:4][C:3]=1[O:2][CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1183VanillinHCID 7410Acetophenone

생성물 1

HCID 1460513-(4-Hydroxy-3-methoxyphenyl)-1-phenyl-2-propen-1-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

3-methoxy-4-hydroxybenzaldehyde (20 gm, 0.132 mol) was added to the solution of acetophenone (20 gm, 0.125 mol) dissolved in acetic acid (20 mL) in a round bottom flask with constant stirring. Temperature of reaction was maintained below 15° C. with Occasional shaking for 200 hrs. Reaction mixture was poured in ice cold water and the product was extracted with chloroform. Chloroform extract was distilled under reduced pressure and the residue was chromatographed on SiO2 gel to obtain 1. m.p. 91° C.

후처리

  1. customTemperature of reaction
  2. temperaturewas maintained below 15° C.
  3. customReaction mixture
  4. additionwas poured in ice cold water
  5. extractionthe product was extracted with chloroform
  6. extractionChloroform extract
  7. distillationwas distilled under reduced pressure
  8. customthe residue was chromatographed on SiO2 gel
  9. customto obtain 1

출처 및 근거

ORD 기록
ord-979f840647cc40cb89eb9b42809b5ac6
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09192589B2

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