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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703476Generated: October 30, 2026

2-Thiophenesulfonyl chloride → HCID 3078271, compound

https://huagongshe.com/reaction/703476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantHCID 14369013HCID 14369013—
SolventDichloromethaneHCID 6344—
ProductHCID 3078271HCID 307827173.2%

Reaction Steps

A solution of 2.87 g (=0.015 mol) thiophene-2-sulfonyl chloride in 20 ml dichloromethane was added dropwise with ice cooling to a solution of 3.5 g (=0.014 mol) 7-benzyl-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane (=substance No. C8 in the following Table (C)) in 40 ml dichloromethane. Then the ice bath was removed and the reaction mixture stirred further for 3 hours at room temperature. The reaction mixture was then made alkaline by adding aqueous sodium hydroxide solution, the aqueous phase was separated and extracted twice with dichloromethane. The combined dichloromethane phases were dried over magnesium sulfate and the solvent was evaporated. 4.0 g of the title compound (base) were thereby obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983611
Source datasetuspto-grants-1991_01
ORD IDord-09176414a74e4cb38660591338e9f5fb
Source noteuspto-grants-1991_01