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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965015Generated: October 30, 2026

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

https://huagongshe.com/reaction/965015

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 a suspension of 24 g of paraformaldehyde (0.8 mole) and 86.4 g of chlorotrimethylsilane (1.6 moles) in 200 mL of 1,2-dichloroethane was added 0.8 ml anhydrous tin(IV) chloride and the resulting solution stirred on a steam bath for one hour. 4-Isopropyl-6-methoxysaccharin (51.4 g, 0.2 mole) 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 50 mL of 2N sodium hydroxide solution, dried over anhydrous magnesium sulfate and concentrated under vacuum. The residue was purified by crystallization from ethyl acetate/hexane to give 57 g (87%) of 2-chloromethyl-4-isopropyl-6-methoxysaccharin, m.p. 151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773456
Source datasetuspto-grants-1998_06
ORD IDord-58be83912846403cb1806d2dcee2ddfe
Source noteuspto-grants-1998_06