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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746202Generated: October 31, 2026

Potassium tert-butoxide → HCID 178516555, compound

https://huagongshe.com/reaction/1746202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86660133HCID 86660133—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178516555HCID 17851655591%

Reaction Steps

Dimethyl-thiocarbamic acid S-(2-acetyl-5-fluoro-phenyl) ester (2.7 g, 11.2 mmol) was dissolved in dry THF (15 mL) and transferred via cannula to a flask containing 1M potassium tert-butoxide in THF (22.4 mL). The reaction was permitted to for 4 h at ambient temperature. The reaction mixture was concentrated in vacuo and dissolved in water. The aqueous layer was extracted with diethyl ether and the organic phase was discarded. The aqueous portion was acidified to pH 3 with 1N HCl, the precipitate collected via filtration and air dried to provide 7-fluoro-4-hydroxy-thiochromen-2-one (2.0 g, 91%) which was used without further purification. MS ESI(−) m/e: 195.209 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149476B2
Source datasetuspto-grants-2015_10
ORD IDord-14d852283bb641429718bff29b2757cd
Source noteuspto-grants-2015_10