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Monobenzone → Ethyl [4-(Benzyloxy)phenoxy]acetate

HRID 2119827
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HRID 2119827 반응식
[CH2:1]([O:3][C:4](=[O:7])[CH2:5]Br)[CH3:2].[CH2:8]([O:15][C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][CH:17]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH2:1]([O:3][C:4](=[O:7])[CH2:5][O:22][C:19]1[CH:18]=[CH:17][C:16]([O:15][CH2:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)=[CH:21][CH:20]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7638MonobenzoneHCID 7748Ethyl bromoacetateHCID 11430Potassium Carbonate

생성물 1

HCID 734886Ethyl [4-(Benzyloxy)phenoxy]acetate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Ethylbromoacetate (4.17 g, 25 mmol) was added to a mixture of 4-benzyloxyphenol (5.00 g, 25 mmol) and K2CO3 (3.50 g, 25 mmol) in DMF (75 mL) and stirred for 20 hours at ambient temperature. The mixture was then concentrated in vacuo and the residue partitioned between water and EtOAc. The aqueous phase was further extracted with 2×50 mL of EtOAc and the combined extracts were washed with 2×50 mL of water and dried over Na2SO4. Concentration of the organic solution in vacuo left 7.00 g (97%) of product as a white solid. m.p. 65-68° C.

후처리

  1. concentrationThe mixture was then concentrated in vacuo
  2. customthe residue partitioned between water and EtOAc
  3. extractionThe aqueous phase was further extracted with 2×50 mL of EtOAc
  4. washthe combined extracts were washed with 2×50 mL of water
  5. dry with materialdried over Na2SO4
  6. waitConcentration of the organic solution in vacuo left 7.00 g (97%) of product as a white solid

출처 및 근거

ORD 기록
ord-0df8950e2cca47ffaefe3e5ba7e76d52
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06686372B2

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