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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768698Generated: October 30, 2026

Formaldehyde → 2-(Chloromethyl)-4-isopropyl-6-methoxybenzo[D]isothiazol-3(2H)-one 1,1-dioxide

https://huagongshe.com/reaction/1768698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTin tetrachlorideHCID 24287—
Reactant4-Isopropyl-6-methoxysaccharinHCID 10147362—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2-(Chloromethyl)-4-isopropyl-6-methoxybenzo[D]isothiazol-3(2H)-one 1,1-dioxideHCID 999517387%

Reaction Steps

To ba suspension of paraformaldehyde (24 g) and chlorotrimethylsilane (86.4 g) in 1,2-dichloroethane (200 mL) was added dry tin(IV) chloride (0.8 mL) and the resulting solution was stirred on a steam bath for one hour. 4-Isopropyl-6-methoxysaccharin (51.4 g) was added to the clear solution and the mixture was refluxed for 18 hours, cooled to room temperature and poured into water. The organic layer was separated, washed with aqueous sodium hydroxide solution (2N, 50 mL), dried over magnesium sulfate and concentrated under vacuum. The residue was crystallized from ethyl acetate-hexane to give 2-chloromethyl-4-isopropyl-6-methoxysaccharin (57 g, 87% yield, m.p. 151° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378720
Source datasetuspto-grants-1995_01
ORD IDord-f50d2647692448a2b27df5d994e92f31
Source noteuspto-grants-1995_01