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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169711Generated: October 30, 2026

Water → Ethyl [(4-aminophenyl)(methyl)oxido-sulfanylidene]carbamate

https://huagongshe.com/reaction/1169711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant(RS)-N-(ethoxycarbonyl)-S-methyl-S-(4-nitrophenyl)sulfoximideHCID 59674069—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductEthyl [(4-aminophenyl)(methyl)oxido-sulfanylidene]carbamateHCID 44122615100%

Reaction Steps

A solution of 8.70 g (32.0 mmol) (RS)—N-(ethoxycarbonyl)-S-methyl-S-(4-nitro-phenyl)sulfoximide in 650 ml THF is slowly treated at room temperature with 435 ml of a 10% solution of Ti(III)Cl in approximately 10% hydrochloric acid (Aldrich). The mixture is stirred at room temperature for 4 hours and then cooled to 0° C. 450 ml of a 32% NaOH solution are added dropwise. During this, the reaction mixture is periodically diluted by the addition of water and ethyl acetate. It is treated with 500 ml ethyl acetate and the organic phase is separated. The mushy aqueous phase is extracted with ethyl acetate. The combined organic phases are washed with dilute NaCl solution, dried (Na2SO4), filtered and concentrated. 8.05 g (ca. 32.0 mmol) of the product is obtained, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825128B2
Source datasetuspto-grants-2010_11
ORD IDord-a8b1fd08f47343d2b315df070d8aa0c4
Source noteuspto-grants-2010_11