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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363723Generated: October 31, 2026

Triethylamine → HCID 86753745, compound

https://huagongshe.com/reaction/363723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant4-Methylbenzene-1-sulfonic acid--5,6,7,7a-tetrahydrothieno[3,2-c]pyridin-2(4H)-one (1/1)HCID 45108320—
SolventDichloromethaneHCID 6344—
ProductHCID 86753745HCID 86753745—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 2.00 g of 5,6,7,7a-tetrahydro-4H-thieno[3,2-c]pyridin-2-one-p-toluenesulfonate, 1.84 g of tert-butyldiphenylchlorosilane, 0.66 g of triethylamine and 7 ml of methylene chloride was stirred at room temperature (20° C.) for 3 hours. The produced 2-(tert-butyldiphenylsilyloxy)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-p-toluenesulfonate was not isolated, and 0.96 g of 2-chlorobenzyl chloride and 1.21 g of triethylamine were added thereto. The mixture was allowed to react at room temperature (20° C.) for 1.5 hours by further stirring and then left to stand overnight to obtain a reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874581
Source datasetuspto-grants-1999_02
ORD IDord-f736854bcaad48889bca451481b0bad5
Source noteuspto-grants-1999_02