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Water → HCID 20496827, 화합물

HRID 894433
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HRID 894433 반응식
[C:1]1([CH2:7][CH2:8][O:9][CH2:10][CH:11]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([O:19]C)[CH:14]=2)[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C=CC=CC=1.Cl.N1C=CC=CC=1.O>CCOCC>[C:1]1([CH2:7][CH2:8][O:9][CH2:10][CH:11]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([OH:19])[CH:14]=2)[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

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HCID 962WaterHCID 1049PyridineHCID 10176127Pyridinium chlorideHCID 204969232-(3-Methoxyphenyl)propyl 2-Phenylethyl Ether

생성물 1

HCID 20496827HCID 20496827, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
190 °C

실험 절차

A mixture of 2-(3-methoxyphenyl)propyl 2-phenylethyl ether (176 mg., 0.65 mmole), pyridine (0.4 ml., 4.96 mmole) and dry pyridine hydrochloride (4 g., 34.6 mmole) is heated at 190° C. for 6 hours. The reaction mixture is cooled and added to a mixture of water (100 ml.) and ether (150 ml.). The ether extract is washed once with water (50 ml.) and, along with a second ether extract (50 ml.) of the aqueous phase, is dried over magnesium sulfate and evaporated to an oil. The oil is purified via preparative layer chromatography on silica gel plates, eluted six times with 30% ether-pentane to yield the title product.

후처리

  1. temperatureThe reaction mixture is cooled
  2. extractionThe ether extract
  3. washis washed once with water (50 ml.) and, along with a second ether
  4. extractionextract (50 ml.) of the aqueous phase
  5. dry with materialis dried over magnesium sulfate
  6. customevaporated to an oil
  7. customThe oil is purified via preparative layer chromatography on silica gel plates
  8. washeluted six times with 30% ether-pentane

출처 및 근거

ORD 기록
ord-88fb5f0cba6f4381911021faf99df568
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04283569

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