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Pyridine → 2-Chloro-5-cyano-2,3-dihydro-3,3-dimethylbenzofuran

HRID 444086
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HRID 444086 반응식
S(Cl)([Cl:3])=O.[C:5]([C:7]1[CH:8]=[CH:9][C:10]2[O:14][CH:13](O)[C:12]([CH3:17])([CH3:16])[C:11]=2[CH:18]=1)#[N:6].N1C=CC=CC=1>ClCCl>[Cl:3][CH:13]1[C:12]([CH3:17])([CH3:16])[C:11]2[CH:18]=[C:7]([C:5]#[N:6])[CH:8]=[CH:9][C:10]=2[O:14]1
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 205362002-Hydroxy-3,3-dimethyl-2,3-dihydrobenzofuran-5-carbonitrile

생성물 1

HCID 205362092-Chloro-5-cyano-2,3-dihydro-3,3-dimethylbenzofuran수율 78.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Thionyl chloride (9.3 g) in dichloromethane (10 ml) was added dropwise with stirring and cooling to 5-cyano-2,3-dihydro-3,3-dimethyl-2-hydroxybenzofuran (11.3 g) prepared as in Example 10 and pyridine (6.2 g) in dichloromethane (60 ml). The mixture was stirred for 2 hours at room temperature prior to washing with water, dilute sodium hydroxide solution and water again, drying over magnesium sulphate and evaporating under vacuum. Recrystallisation from toluene and petroleum ether (bp 80°-100° C.) gave 9.7 g of the title compound, mp 105°-106° C.

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후처리

  1. stirringThe mixture was stirred for 2 hours at room temperature
  2. washto washing with water, dilute sodium hydroxide solution and water again
  3. dry with materialdrying over magnesium sulphate
  4. customevaporating under vacuum
  5. customRecrystallisation from toluene and petroleum ether (bp 80°-100° C.)

출처 및 근거

ORD 기록
ord-bfbace54bae049b5aaea04c2f50965e3
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263037

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