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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363722Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 86753744, compound

https://huagongshe.com/reaction/363722

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant5,6,7,7a-Tetrahydrothieno[3,2-c]pyridin-2(4H)-oneHCID 13748463—
SolventDichloromethaneHCID 6344—
ProductHCID 86753744HCID 86753744—

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-butyldimethylchlorosilane, 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, 5.90 g of 2-chloro-α-methoxycarbonylbenzyl bromide and 3.02 g of triethylamine were added thereto, and the mixture was allowed to react.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874581
Source datasetuspto-grants-1999_02
ORD IDord-e7f1f02c142945aeacad3ea3cf4f5251
Source noteuspto-grants-1999_02