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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363721Generated: October 28, 2026

Triethylamine → p-Toluenesulfonic acid

https://huagongshe.com/reaction/363721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 15392095HCID 15392095—
Reactant4-Methylbenzene-1-sulfonic acid--5,6,7,7a-tetrahydrothieno[3,2-c]pyridin-2(4H)-one (1/1)HCID 45108320—
SolventDichloromethaneHCID 6344—
Productp-Toluenesulfonic acidHCID 6101—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 5.00 g of 5,6,7,7a-tetrahydro-4H-thieno[3,2 -c]pyridin-2-one-p-toluenesulfonate, 2.47 g of tert-butyl-dimethylchlorosilane, 1.66 g of triethylamine and 15 ml of methylene chloride was stirred at room temperature (20° C.) for 3 hours. The produced 2-(tert-butyldimethylsilyloxy)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine.p-toluenesulfonate was not isolated, 2.40 g of 2-chlorobenzyl chloride and 3.02 g of triethylamine were added thereto, and the mixture was allowed to react under stirring at 40° C. for 8 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874581
Source datasetuspto-grants-1999_02
ORD IDord-7dad5dac702e483eb0de331a78fc79f7
Source noteuspto-grants-1999_02