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Diethyl Ether → 3-Phenoxyphenyl ethyl ketone

HRID 1907018
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HRID 1907018 반응식
[O:1]([C:8]1[CH:9]=[C:10]([CH:14]([OH:17])[CH2:15][CH3:16])[CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OCC)C.[Cr](O)(O)(=O)=O.C(=O)([O-])[O-].[Na+].[Na+]>O>[O:1]([C:8]1[CH:9]=[C:10]([C:14](=[O:17])[CH2:15][CH3:16])[CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl Ether2회HCID 10340Sodium CarbonateHCID 24425Chromic AcidHCID 151854771-(3-Phenoxyphenyl)propan-1-ol

생성물 1

HCID 108679943-Phenoxyphenyl ethyl ketone

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 35 g of 1-(3-phenoxyphenyl)propan-1-ol and 50 ml of ethyl ether is treated with 1.1 equivalants of chromic acid, which is added dropwise over a 30 minute period. The reaction mixture is allowed to warm to 20°-25° C. and stirred for about 2 hours. Then the reaction mixture is added to a mixture of 25 ml of ethyl ether and 50 ml of water, and sodium carbonate is slowly added to neutralize the acid. The phases are separated and the aqueous phase is reextracted twice with ethyl ether. The ethereal extracts are combined and evaporated under reduced pressure to yield 1-(3-phenoxyphenyl)-propan-1-one as an oil.

후처리

  1. additionis added dropwise over a 30 minute period
  2. temperatureto warm to 20°-25° C.
  3. additionis slowly added
  4. customThe phases are separated
  5. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-599bb8e57ab140b9a2ddb266807e6824
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04654438

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