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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606304생성일: 2026년 10월 25일

Thionyl Chloride → 1-Chloro-4-chloromethyl-3-methyl-isoquinoline

https://huagongshe.com/reaction/606304

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물Aluminium lithium hydrideHCID 21226445—
반응물1-Chloro-3-methyl-isoquinoline-4-carbaldehydeHCID 86615929—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-Chloro-4-chloromethyl-3-methyl-isoquinolineHCID 8661593190%

반응 단계

LAH (3.6 ml of 1M in THF, 3.62 mmol) is added to a solution of 1-chloro-3-methyl-isoquinoline-4-carbaldehyde (744 mg, 3.62 mmol) in THF (10 ml) at 0° C. After stirring for 30 min at ambient temperature, the mixture is quenched with small amounts of saturated sodium sulfate and filtered through a pad of celite. The filtrate is concentrated in vacuo to give the crude alcohol. SOCl2 (13 ml of 2M in DCM, 25 mmol) is added to a solution of the crude alcohol in DCM (5 ml). After stirring for 1 h at room temperature, the mixture is concentrated in vacuo and the residue is chromatographed on silica gel to give 737 mg of 1-chloro-4-chloromethyl-3-methyl-isoquinoline. 1H NMR (CDCl3) 8.44 (d, 1H), 8.18 (d, 1H), 8.02 (t, 1H), 7.82 (t, 1H), 5.03 (s, 2H), 3.00 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915288B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-5c0e840b92554b8ba569216e3d66857b
출처 메모uspto-grants-2011_03