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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891084Generated: November 1, 2026

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

https://huagongshe.com/reaction/1891084

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 numberUS08507510B2
Source datasetuspto-grants-2013_08
ORD IDord-896d8f4a81824f55937d87d0d5620201
Source noteuspto-grants-2013_08