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Phenacyl bromide → 2-Propyl-3-(2-phenyl-2-oxoethoxy)phenol

HRID 342762
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HRID 342762 반응식
[CH2:1]([C:4]1[C:10]([OH:11])=[CH:9][CH:8]=[CH:7][C:5]=1[OH:6])[CH2:2][CH3:3].C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:19][C:20]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:21]>CN(C=O)C>[CH2:1]([C:4]1[C:10]([O:11][CH2:19][C:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[O:21])=[CH:9][CH:8]=[CH:7][C:5]=1[OH:6])[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6259Phenacyl bromideHCID 10796Cesium carbonateHCID 2620601,3-Benzenediol, propyl-

생성물 1

HCID 543761242-Propyl-3-(2-phenyl-2-oxoethoxy)phenol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a solution of 2-propyl resorcinol (178.27 g; 1.171 mol) in dry DMF (1200 mL) was added cesium carbonate (104.95 g; 322.12 mmol). The mixture was stirred at room temperature and treated dropwise with a solution of 2-bromoacetophenone (58.29 G; 292.84 mmol) in dry DMF (500 mL) over 2 hours. The was stirred at ambient temperature for 64 hours. The reaction mixture was partitioned between isopropyl acetate and water. The aqueous was adjusted to pH 13 by addition of aq. 5N sodium hydroxide. The organic was dried over magnesium sulfate, filtered and evaporated to a residue. The residue was dissolved in methylene chloride (110 mL) and hexane (350 mL) and heated to reflux. The solution was cooled to -10° C. Stirring was continued for 1 hour. The title compound was recovered by filtration.

후처리

  1. stirringThe was stirred at ambient temperature for 64 hours
  2. customThe reaction mixture was partitioned between isopropyl acetate and water
  3. additionThe aqueous was adjusted to pH 13 by addition of aq. 5N sodium hydroxide
  4. dry with materialThe organic was dried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated to a residue
  7. dissolutionThe residue was dissolved in methylene chloride (110 mL)
  8. temperaturehexane (350 mL) and heated to reflux
  9. temperatureThe solution was cooled to -10° C
  10. stirringStirring
  11. filtrationThe title compound was recovered by filtration

출처 및 근거

ORD 기록
ord-b59cb8e48faa4c4d85e0bc621804da61
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859051

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