Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910496Generated: November 1, 2026

2-(Chloroacetyl)thiophene → HCID 86672934, compound

https://huagongshe.com/reaction/1910496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloroacetyl)thiopheneHCID 2757925—
ReactantHCID 70925878HCID 70925878—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672934HCID 8667293474%

Reaction Steps

2-Chloro-1-(thiophen-2-yl)ethanone (30.2 mg, 0.19 mmol) was added to a solution of (R)-thiophen-2-ylmethyl quinuclidin-3-ylcarbamate (50.0 mg, 0.19 mmol) in EtOAc (3 ml). The reaction was stirred at room temperature overnight. The solvent was removed, and the residue was triturated in Et2O, filtered and dried to give (R)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-3-((thiophen-2-ylmethoxy)carbonylamino)-1-azoniabicyclo[2.2.2]octane chloride (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-b6627482a42e46158e60b9f8c51d8bc2
Source noteuspto-grants-2013_12