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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395282Generated: October 31, 2026

Thionyl Chloride → HCID 20340826, compound

https://huagongshe.com/reaction/1395282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20340829HCID 20340829—
ProductHCID 20340826HCID 20340826—

Reaction Steps

11.4 g. of 4,6-dichloroquinoline-3-methanol (0.05 mol.) are added in portions to 150 ml. of thionyl chloride. The reaction mixture is allowed to stand for 24 hours at room temperature. Then the solution is filtered and the excess thionyl chloride removed by a rotary evaporator. The residue is triturated with water, filtered off, washed again with water and dried in a desiccator over P2O5 to obtain 3-chloromethyl-4,6-dichloroquinoline; yield: 11.5 g. (93.5%); m.p. 102°-105°. Recrystallization from cyclohexane does not change the melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202985
Source datasetuspto-grants-1980_05
ORD IDord-b0be73cef6d947a8a692b7f493874768
Source noteuspto-grants-1980_05