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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036835Generated: October 25, 2026

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

https://huagongshe.com/reaction/1036835

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 numberUS08546431B2
Source datasetuspto-grants-2013_10
ORD IDord-a16b3bbf5b4a4a3d89dcba62f28b8a28
Source noteuspto-grants-2013_10