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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948887Generated: October 25, 2026

tert-Butyl mercaptan → Ethyl 4-(tert-butylthio)-3-oxobutanoate

https://huagongshe.com/reaction/1948887

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(tert-butylthio)-3-oxobutanoateHCID 10465978—

Reaction Steps

Ethyl 4-chloroacetoacetate (7.5 mL, 51.9 mmol), 2-methyl-2-propanethiol (5.6 mL, 49.7 mmol), triethylamine (10.8 mL, 77.4 mmol), and catalytic tetrabutylammonium bromide were dissolved in THF (250 mL) and stirred at room temperature overnight. Silica gel was added, and the mixture was concentrated and filtered over a plug of silica gel to obtain the desired product (B-1), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399666B2
Source datasetuspto-grants-2013_03
ORD IDord-5ec9328f963847768482c3c278621ee9
Source noteuspto-grants-2013_03