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Hydrochloric Acid → 2-(5-Fluoro-2-hydroxyphenyl)-2-(5-fluoro-2-methoxyphenyl)propane

HRID 1413856
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반응식

HRID 1413856 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][CH3:13])=[C:6]([C:8](O)([CH3:10])[CH3:9])[CH:7]=1.[F:14][C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=1.Cl>CCOCC>[F:14][C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[C:17]([C:8]([C:6]2[CH:7]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:12][CH3:13])([CH3:10])[CH3:9])[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 97324-FluorophenolHCID 222848882-(5-Fluoro-2-methoxyphenyl)propan-2-ol

생성물 1

HCID 202910912-(5-Fluoro-2-hydroxyphenyl)-2-(5-fluoro-2-methoxyphenyl)propane수율 43%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

2-(5-fluoro-2-methoxyphenyl)propan-2-ol (6 g) was added in small portions to a melt of 4-fluorophenol (12 g) and concentrated hydrochloric acid (10 days) at 90° C. The mixture was stirred at this temperature overnight and was then cooled and dissolved in ether. The excess of p-fluorophenol was removed by extraction with 5% aqueous sodium hydroxide solution. The alkali insoluble material crystallised from hexane to give 2-(5-fluoro-2-hydroxyphenyl)-2-(5-fluoro-2-methoxyphenyl) propane (3.9 g) as colourless prisms; m.p. 90° C.

후처리

  1. temperaturewas then cooled
  2. customThe excess of p-fluorophenol was removed by extraction with 5% aqueous sodium hydroxide solution
  3. customThe alkali insoluble material crystallised from hexane

출처 및 근거

ORD 기록
ord-e736f129532f4a72b644bf67ccbcaadb
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04251546

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