Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620175Generated: October 28, 2026

Thionyl Chloride → HCID 68182227, compound

https://huagongshe.com/reaction/1620175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 68182185HCID 68182185—
SolventDichloromethaneHCID 6344—
ProductHCID 68182227HCID 6818222784%

Reaction Steps

To a solution of (5-methoxyquinolin-3-yl)methanol CCH 34144-3 (80 mg, 423 μmol) in dry CH2Cl2 (12 mL) at 0° C. under N2 in a 25 mL round-bottomed flask equipped with a magnetic stirrer was added dropwise SOCl2 (0.60 mL, 8.27 mmol) and the mixture was stirred for 2 h at RT. The volatiles were then removed at 40° C. under vacuum and the residue was taken up in CH2Cl2 (20 mL) before concentration back to dryness at 40° C. under vacuum (done 3 times) to give 3-(chloromethyl)-5-methoxyquinoline hydrochloride CCH 341448 as an off-white solid (87 mg, 84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-19acb9766ac243b1b74a43163463a6fa
Source noteuspto-grants-2014_07