Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910493Generated: November 4, 2026

2-(Chloroacetyl)thiophene → HCID 86672928, compound

https://huagongshe.com/reaction/1910493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloroacetyl)thiopheneHCID 2757925—
ReactantHCID 70673881HCID 70673881—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672928HCID 8667292872.7%

Reaction Steps

2-Chloro-1-(thiophen-2-yl)ethanone (12.0 mg, 0.07 mmol) was added to a solution of (4-methoxyphenyl)(phenyl)methyl(R)-quinuclidin-3-ylcarbamate (22.0 mg, 0.06 mmol, prepared as in example 3) in ethyl acetate (2 ml). The reaction was stirred at room temperature for two days. The reaction was evaporated to dryness. The crude was purified by flash chromatography (DCM/MeOH=95/5) to obtain (3R)-3-(((4-methoxyphenyl)(phenyl)methoxy)carbonylamino)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane chloride (23 mg, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-3687e6c7d1684c47b3c5ee1fcefcfa57
Source noteuspto-grants-2013_12