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Pyridinium chloride → 2-(3-Hydroxyphenyl)-5-phenylpentane

HRID 225185
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반응식

HRID 225185 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16]C=2)[CH:6]=[CH:7][CH:8]=1.Cl.N1C=CC=C[CH:22]=1>Cl.O>[OH:2][C:3]1[CH:4]=[C:5]([CH:9]([CH2:10][CH2:11][CH2:12][C:13]2[CH:14]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH3:22])[CH:6]=[CH:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 10176127Pyridinium chlorideHCID 86736615HCID 86736615, 화합물

생성물 1

HCID 204968222-(3-Hydroxyphenyl)-5-phenylpentane

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

반응 조건

온도
190 °C

실험 절차

A mixture of 2-(3-methoxyphenyl-5-phenylpentane (20 g.) and pyridine hydrochloride (94 g.) under nitrogen is heated to 190° C. for 2 hours with vigorous stirring. The reaction mixture is cooled, dissolved in 6 N hydrochloric acid (200 ml.) and diluted with water to 600 ml. The aqueous solution is extracted with ethyl acetate (4×100 ml.), the ethyl acetate extracts dried over sodium sulfate and concentrated under vacuum to yield the crude product which is purified by silica gel chromatography to yield 2-(3-hydroxyphenyl)-5-phenylpentane as an oil.

후처리

  1. temperatureThe reaction mixture is cooled
  2. extractionThe aqueous solution is extracted with ethyl acetate (4×100 ml.)
  3. dry with materialthe ethyl acetate extracts dried over sodium sulfate
  4. concentrationconcentrated under vacuum
  5. customto yield the crude product which
  6. customis purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-17fddf462ef841bca3de37608d0ab90f
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04235913

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