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2-Bromoethanol → 4-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate

HRID 989989
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인쇄 미리보기

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HRID 989989 반응식
[OH:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:27][CH2:28][OH:29]>>[OH:29][CH2:28][CH2:27][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[O:7])=[CH:18][CH:19]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 108982-BromoethanolHCID 11430Potassium CarbonateHCID 12119266Benzoic acid, 4-hydroxy-, (4-methoxyphenyl)methyl ester

생성물 1

HCID 220358874-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate

반응 조건

온도
80 °C

실험 절차

To a solution of 4-methoxybenzyl 4-hydroxybenzoate (7.0 g, 27 mmole) in dry N,N-dimethylforuiamide (50 ml) was added potassium carbonate (4.15 g, 30 mmole) and 2-bromoethanol. The mixture was stirred 48 hours at 80° C., evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed five times with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with hexane/ethyl acetate.

후처리

  1. customevaporated under reduced pressure and ethyl acetate and water
  2. additionwere added
  3. washThe organic phase was washed five times with water
  4. dry with materialdried with sodium sulfate
  5. customThe solution was evaporated under reduced pressure
  6. customthe product was isolated by silica gel column chromatography with hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-43ac2423fb2841e9b2440e8d5541f1ac
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06458772B1

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