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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391477Generated: November 3, 2026

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

https://huagongshe.com/reaction/1391477

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) of (RS)-N-(ethoxycarbonyl)-S-methyl-S-(4-nitrophenyl)sulfoximide in 650 ml of THF is slowly mixed at room temperature with 435 ml of a 10% solution of Ti(III)Cl in approximately 10% hydrochloric acid (Aldrich). The batch is stirred for 4 hours at room temperature and then cooled to 0° C. 450 ml of a 32% NaOH solution is added in drops. In this case, the reaction mixture is now diluted by the addition of water and ethyl acetate. It is mixed with 500 ml of ethyl acetate, and the organic phase is separated. The pulpy, aqueous phase is extracted from ethyl acetate. The combined organic phases are washed with dilute NaCl solution, dried (Na2SO4), filtered and concentrated by evaporation. 8.05 g (about 32.0 mmol) of the product is obtained, and said product is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338958B2
Source datasetuspto-grants-2008_03
ORD IDord-cdcc87add8eb4785aa0a0e929033b272
Source noteuspto-grants-2008_03