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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891063Generated: October 31, 2026

Ethyl Acetate → 851008-24-7

https://huagongshe.com/reaction/1891063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant1-(S-Methanesulfonimidoyl)-3-nitrobenzeneHCID 59674053—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product851008-24-7HCID 59674075—

Reaction Steps

A solution of 200 mg (1.00 mmol) of (RS)—S-methyl-S-(3-nitrophenyl)sulfoximide in 20 ml of THF is mixed at room temperature with 8 ml of an approximately 10% solution of Ti(III)Cl in 20-30% hydrochloric acid. After 3 hours, another 2 ml of the approximately 10% solution of Ti(III)Cl in 20-30% hydrochloric acid is added and stirred overnight at room temperature. The batch is made basic with 1N NaOH solution and mixed with ethyl acetate. It is filtered, and the filter cakes are washed with ethyl acetate/MeOH (3:2). The organic solvent is drawn off in a rotary evaporator, and the residue is extracted from ethyl acetate. The combined organic phases are dried (Na2SO4), filtered and concentrated by evaporation. The residue that is obtained is purified by chromatography (DCM/EtOH 95:5). 82 mg (0.48 mmol, corresponding to 48% of theory) of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507510B2
Source datasetuspto-grants-2013_08
ORD IDord-4e3dc7f59bba46e0878b3d72ee17ccb5
Source noteuspto-grants-2013_08