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2-Propen-1-one, 1-(hydroxyphenyl)-3-phenyl- → HCID 11805918, 화합물

HRID 1462954
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HRID 1462954 반응식
O[C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4](=[O:13])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[BH4-].[Na+]>C(O)C>[O:13]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]1[C:3]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 146112-Propen-1-one, 1-(hydroxyphenyl)-3-phenyl-HCID 4311764Sodium borohydride

생성물 1

HCID 11805918HCID 11805918, 화합물수율 75.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2'-Hydroxychalcone (9.0 g) was stirred with ethanol (100 ml) at room temperature whilst sodium borohydride (3.05 g) was added in small portions. After 2 hr. stirring the colourless solution was evaporated to dryness and acetic acid (100 ml) added. Toluene sulphonic acid (1.0 g) was added and the solution was heated on the steam bath for 30 min. The solution was diluted with water and extracted with toluene. The extract was washed with saturated sodium bicarbonate solution, dried over magnesium sulphate, and evaporated. The residue was chromatographed on neutral alumina to yield flav-3-ene (6.3 g) as an oil, identified by its n.m.r. spectrum. The multiplet at 5.8 p.p.m. is characteristic of flav-3-enes.

후처리

  1. additionwas added in small portions
  2. customwas evaporated to dryness and acetic acid (100 ml)
  3. additionadded
  4. additionToluene sulphonic acid (1.0 g) was added
  5. temperaturethe solution was heated on the steam bath for 30 min
  6. additionThe solution was diluted with water
  7. extractionextracted with toluene
  8. washThe extract was washed with saturated sodium bicarbonate solution
  9. dry with materialdried over magnesium sulphate
  10. customevaporated
  11. customThe residue was chromatographed on neutral alumina

출처 및 근거

ORD 기록
ord-fa1ffa66b37f42fea7f801760edf3c61
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461907

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