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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520359Generated: October 26, 2026

tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate

https://huagongshe.com/reaction/520359

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
ReactantEthyl 4-fluoro-3,3-dimethyl-2-oxobutanoateHCID 86690078—
CatalystHCID 178477244HCID 178477244—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoateHCID 8669007930.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoate (2.3 g, 13.05 mmol) in THF (20 mL) was added (S)-2-methylpropane-2-sulfinamide (1.899 g, 15.67 mmol) and tetraethoxytitanium (5.91 mL, 26.1 mmol). The reaction mixture was heated at 65° C. for 6 h. The reaction mixture was cooled down, diluted with EtOAc and sat. NaCl (40 mL) and stirred at rt for 0.5 h. The solid was filtered and washed with water and EtOAc. The filtrate was separated and the organic layer was washed with water, sat. NaCl, dried (MgSO4) and purified by flash chromatography (EtOAc/hexane) to afford (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate (1.1 g). 1H NMR (400 MHz, CDCl3) δ ppm 4.46-4.53 (1H, m), 4.28-4.42 (3H, m), 1.59 (3H, s), 1.21-1.31 (15H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326973B2
Source datasetuspto-grants-2016_05
ORD IDord-123710cb3b9642a2a1939182945b1418
Source noteuspto-grants-2016_05