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Thionyl Chloride → HCID 23018027, 화합물

HRID 1788399
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HRID 1788399 반응식
S(Cl)([Cl:3])=O.[F:5][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:15]=1[N:14]=[C:13]([CH3:16])[CH:12]=[C:11]2[CH2:17]O>C(Cl)(Cl)Cl>[ClH:3].[Cl:3][CH2:17][C:11]1[C:10]2[C:15](=[C:6]([F:5])[CH:7]=[CH:8][CH:9]=2)[N:14]=[C:13]([CH3:16])[CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23017958HCID 23017958, 화합물

생성물 1

HCID 23018027HCID 23018027, 화합물수율 100.8%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

At 0° C., 0.75 mL (10.4 mmol) of thionyl chloride was dropped into a solution of 1.00 g (5.23 mmol) of (8-fluoro-2-methylquinolin-4-yl)methanol obtained in the above 1) in chloroform (12 mL) and stirred for 15 hours at room temperature. The reaction mixture was removed under a reduced pressure and then, the residue was washed with ethyl acetate to obtain 1.29 g (yield 100%) of 4-chloromethyl-8-fluoro-2-methylquinoline hydrochloride (XII-124). Its physical property is shown below.

후처리

  1. customThe reaction mixture was removed under a reduced pressure
  2. washthe residue was washed with ethyl acetate

출처 및 근거

ORD 기록
ord-a4a0988fa12e4acb83ea520bc0e7ed4c
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07511144B2

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