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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615820Generated: November 1, 2026

Methanol → HCID 66865026, compound

https://huagongshe.com/reaction/1615820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
ReactantEthyl 5-(3,5-difluorophenyl)-5-oxopentanoateHCID 24727360—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 66865026HCID 66865026—

Reaction Steps

To a solution of ethyl 5-(3,5-difluorophenyl)-5-oxovalerate (5.00 g, 19.5 mmol) and (S)-2-methylpropane-2-sulfinamide (2.88 g, 23.8 mmol) in THF (123 mL) was added titanium tetraethoxide (8.18 mL, 39.0 mmol). The reaction vessel was quickly sealed and placed into a 60° C. bath for 16 h. After cooling to ambient temperature a septum and nitrogen inlet were attached prior to cooling to 0° C. Sodium borohydride (1.48 g, 39.0 mmol) was then added, and a complete reaction was observed after 1 h. Methyl alcohol was then slowly added until gas evolution had stopped. The reaction mixture was then diluted with brine (60 mL) while experiencing rapid stirring. The resultant slurry was filtered through celite, washing with EtOAc as needed. The combined organics were then washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to give an oil, which was purified by silica gel chromatography, eluting with a gradient of EtOAc:hexanes—10:90 to 50:50, to give the title compound. MS: m/z=362 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765759B2
Source datasetuspto-grants-2014_07
ORD IDord-10d62f08fde34f65ba045ccd293ee57c
Source noteuspto-grants-2014_07