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Pyridine → 2-(3-Chloropropyl)-6-methylphenol

HRID 343484
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HRID 343484 반응식
O[CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:6]=1[OH:12].N1C=CC=CC=1.S(Cl)([Cl:21])=O>O1CCCC1.CN(C)C=O>[Cl:21][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:6]=1[OH:12]
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참가 물질

6

반응물 3

HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 543527972-(3-Hydroxypropyl)-6-methylphenol

생성물 1

HCID 544438172-(3-Chloropropyl)-6-methylphenol

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 8028Tetrahydrofuran용매

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온도
60 °C

실험 절차

To a solution of 2-(3-hydroxypropyl)-6-methylphenol (3.0 g) in tetrahydrofuran (30 mL) were added pyridine (730 μL), thionyl chloride (2 mL) and one drop of N,N-dimethylformamide. After stirring at 60° C. for 2 hours, the reaction mixture was evaporated, and then diethyl ether was added to the residue. The resulting solution was washed with distilled water and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo to give the title compound in quantitative yield.

후처리

  1. customthe reaction mixture was evaporated
  2. additiondiethyl ether was added to the residue
  3. washThe resulting solution was washed with distilled water and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-d12eb7ad3b8d4622b4cc040d6ed8f77d
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05861437

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