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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238132Generated: October 31, 2026

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

https://huagongshe.com/reaction/238132

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)Cl3 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 numberUS08642611B2
Source datasetuspto-grants-2014_02
ORD IDord-512be9e4dc534add8a54083bfaca7446
Source noteuspto-grants-2014_02