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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266485Generated: November 1, 2026

tert-Butanol → HCID 68783725, compound

https://huagongshe.com/reaction/2266485

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantEthyl 3-oxovalerateHCID 78656—
Reactant4-(Methylsulfonyl)benzyl BromideHCID 2733581—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68783725HCID 68783725—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of potassium tert-butoxide (3.9 g) in anhydrous tetrahydrofuran (60 mL) at 0° C. was treated with a mixture of tert-butanol (0.15 mL) and 3-oxopentanoic acid ethyl ester (5.0 g). The mixture was warmed to room temperature and after 30 minutes a solution of 1-bromomethyl-4-methanesulfonylbenzene (8.6 g) in tetrahydrofuran (20 mL) was added and the resulting mixture heated at 70° C. for 17 hours. The mixture was cooled to room temperature and diluted with water (20 mL) and this mixture was extracted with ethyl acetate. The combined extracts were washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified, by column chromatography on silica gel, eluting with a mixture of dichloromethane and ethyl acetate (1:0 to 4:1 by volume) to afford title compound as a white solid, 3.6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-5c56e09a1d8345d4a1cc020ecd3ff708
Source noteuspto-grants-2010_12