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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347809Generated: October 28, 2026

p-Anisoyl chloride → HCID 21084206, compound

https://huagongshe.com/reaction/347809

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-azabicyclo[2.2.1]heptane-3-carboxylateHCID 13258847—
SolventChloroformHCID 6212—
ProductHCID 21084206HCID 2108420674%

Reaction Steps

To a solution of ethyl 2-azabicyclo[2.2.1]heptane-3-carboxylate (181 mg, 1.07 mmol) obtained in Example 1 (b) in chloroform (2 ml) were added triethylamine (0.16 ml, 1.18 mmol) and 4-methoxybenzoyl chloride (201 mg, 1.18 mmol) while being cooled with ice. After a reaction at room temperature for 1 hour, the reaction mixture was washed with 1N hydrochloric acid, saturated sodium bicarbonate water and saturated brine successively, and dried over magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (25%–40% ethyl acetate/hexane), to give ethyl 2-(4-methoxybenzoyl)-2-azabicyclo[2.2.1]heptane-3-carboxylate (239 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176217B2
Source datasetuspto-grants-2007_02
ORD IDord-584d4e11e55b4d63b9352f93bec07687
Source noteuspto-grants-2007_02