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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420866Generated: October 30, 2026

Hydrochloric Acid → 2-(2-Cyanoethyl)-4,5-dimethoxyphenyl dimethylsulphamate

https://huagongshe.com/reaction/420866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(2-Cyanovinyl)-4,5-dimethoxyphenyl dimethylsulphamateHCID 66657579—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Cyanoethyl)-4,5-dimethoxyphenyl dimethylsulphamateHCID 6665749994%

Reaction Conditions

Temperature50 °C

Reaction Steps

Disperse 6.7 g (0.177 mol) of sodium borohydride in 150 ml of THF. Pour in dropwise a suspension of 18.4 g (0.059 mol) of 2-(2-cyanovinyl)-4,5-dimethoxyphenyl dimethylsulphamate in 200 ml of THF. Pour in dropwise 48 ml of methanol. Heat for 3 h at 50° C. and then cool and add 1 g (0.026 mol) of sodium borohydride. Heat the reaction mixture at 50° C. for 1 h and then stir overnight at ambient temperature. Hydrolyse by pouring into the reaction mixture 60 ml of aqueous 4N HCl solution while maintaining the temperature at approximately 20° C. Add 40 g of ice and 30 ml of water and then extract twice with 200 ml of ethyl acetate each time. The organic phase is washed with water and saturated aqueous NaCl solution and then dried over MgSO4, filtered and evaporated to dryness. 17.4 g of title product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097720B2
Source datasetuspto-grants-2012_01
ORD IDord-51643aa5b88c44c7a4c461cfee740ecf
Source noteuspto-grants-2012_01