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Thionyl Chloride → 3-(Chloromethyl)-5-fluorobenzofuran

HRID 1358239
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HRID 1358239 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH:8]=[C:7]([CH2:10]O)[C:6]=2[CH:12]=1.S(Cl)([Cl:15])=O>C(Cl)Cl.CN(C)C=O>[Cl:15][CH2:10][C:7]1[C:6]2[CH:12]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:9][CH:8]=1
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참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 18184309HCID 18184309, 화합물

생성물 1

HCID 181843143-(Chloromethyl)-5-fluorobenzofuran

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

A solution of 5-fluorobenzofuran-3-ylmethanol (14 g) in methylene chloride (250 mL) was treated successively with 5 drops of dimethylformamide and thionyl chloride (28 mL). After stirring for 16 h at room temperature the reaction was concentrated in vacuo giving 3-chloromethyl-5-fluorobenzofuran as an oil (19.4 g).

후처리

  1. concentrationwas concentrated in vacuo

출처 및 근거

ORD 기록
ord-85b6230b51dd41d899267ece7db4995d
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06596722B2

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