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Benzyl 4-Hydroxybenzoate → Benzyl 4-(methoxycarbonylmethoxy)benzoate

HRID 2419378
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반응식

HRID 2419378 반응식
[OH:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:7])=[CH:4][CH:3]=1.Br[CH2:19][C:20]([O:22][CH3:23])=[O:21].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:23][O:22][C:20]([CH2:19][O:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:7])=[CH:4][CH:3]=1)=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7180Benzyl 4-HydroxybenzoateHCID 11430Potassium CarbonateHCID 60984Methyl bromoacetate

생성물 1

HCID 18381591Benzyl 4-(methoxycarbonylmethoxy)benzoate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of benzyl 4-hydroxybenzoate (169.0g.), methyl bromoacetate (122.4g.) and anhydrous potassium carbonate (200g.) in acetone (500ml.) (analytical grade) was stirred and heated under reflux for 16 hours. The mixture was then filtered and the filtrate evaporated in vacuo. The semi-solid residue obtained was separated by filtration. The solid thus obtained was washed with cold (0°-5° C.) petroleum ether (b.p. 60°-80° C.) (50ml.) to give benzyl 4-(methoxycarbonylmethoxy)benzoate, m.p. 63°-66° C.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 16 hours
  3. filtrationThe mixture was then filtered
  4. customthe filtrate evaporated in vacuo
  5. customThe semi-solid residue obtained
  6. customwas separated by filtration
  7. customThe solid thus obtained
  8. washwas washed with cold (0°-5° C.) petroleum ether (b.p. 60°-80° C.) (50ml.)

출처 및 근거

ORD 기록
ord-fe9c123f432d45f7b73369e7e05b86ff
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04105790

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