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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235639Generated: October 29, 2026

Thionyl Chloride → 2-(Chloromethyl)-2H-1,4-benzothiazin-3(4H)-one

https://huagongshe.com/reaction/235639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 3300302HCID 3300302—
SolventChloroformHCID 6212—
Product2-(Chloromethyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 1378462558.7%

Reaction Steps

To a solution of 1.0 g of 2-hydroxymethyl-2H-1,4-benzothiazin-3(4H)-one in 20 ml of chloroform was added 0.9 ml of thionyl chloride, and the mixture was heated for 2 hours under reflux. The mixture was concentrated under reduced pressure and the residue was extracted with ether. The extract was washed with water, dried (MgSO4), and concentrated. The crude product was subjected to a column chromatography on silica-gel (40 g). From the eluate with hexane-ethyl acetate (4:1, v/v) was obtained 640 mg (58.7%) of 2-chloromethyl-2H-1,4-benzothiazin-3(4H)-one as crystals. Recrystallization from ethyl acetate and n-hexane gave needles, m.p. 152°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640916
Source datasetuspto-grants-1987_02
ORD IDord-ed48c1c46f6f4ef5a71cc83f13a17e44
Source noteuspto-grants-1987_02