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Water → 3-Benzoylbenzaldehyde

HRID 358116
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HRID 358116 반응식
[C:1]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12][OH:13])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cr](O)(O)(=O)=O.O>CC(C)=O>[C:1]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=[O:13])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 24425Chromic AcidHCID 127837393-(Hydroxymethyl)benzophenone

생성물 1

HCID 130201683-Benzoylbenzaldehyde

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

3-Benzoylbenzyl alcohol (2.0 g) in acetone (10 ml) was treated dropwise at 15°-20° C. with chromic acid solution. After stirring for 5 minutes, water (50 ml) was added and the mixture extracted with ether. The ethereal solution was washed with saturated Na2CO3, saturated NaCl, dried (Na2SO4), evaporated and distilled; b.p. 160°-170° C./0.08 mm, (1.1 g).

후처리

  1. extractionthe mixture extracted with ether
  2. washThe ethereal solution was washed with saturated Na2CO3, saturated NaCl
  3. dry with materialdried (Na2SO4)
  4. customevaporated
  5. distillationdistilled

출처 및 근거

ORD 기록
ord-e31d2c8775634808a7dcbf3afd28363e
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04464391

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