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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620804Generated: October 31, 2026

tert-Butyl mercaptan → Ethyl 5-(tert-butylsulfanyl)-2,2-dimethyl-4-oxopentanoate

https://huagongshe.com/reaction/1620804

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantEthyl 5-bromo-2,2-dimethyl-4-oxopentanoateHCID 4090969—
SolventHexaneHCID 8058—
ProductEthyl 5-(tert-butylsulfanyl)-2,2-dimethyl-4-oxopentanoateHCID 3576811—

Reaction Conditions

Temperature-2.5 °C

Reaction Steps

To a reaction flask containing tetrahydrofuran (5.0-fold, V/W of starting material) was added 5-bromo-2,2-dimethyl-4-oxo-pentanoic acid ethyl ester (1.0 eq) under nitrogen. The mixture was cooled to a temperature of −5-0° C., and a solution of 2-methyl-2-propanethiol (1.2 eq) and triethylamine (1.25 eq) was added while maintaining the temperature below 0° C. The reaction was stirred at room temperature for 25 hours, and then hexane (3.0-fold, V/W of starting material) was slowly added. After agitating for 30 minutes, the solid material was removed by filtration and washed with 50% ethyl acetate/hexane solution. The filtrate was concentrated under reduced pressure to give the desired product, which was taken on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772495B2
Source datasetuspto-grants-2014_07
ORD IDord-3f005074dc9648be948a40463512051c
Source noteuspto-grants-2014_07