Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729252Generated: November 1, 2026

Acetyl chloride → N-acetyl-N-(9-fluorenyl)-beta-alanin ethyl ester

https://huagongshe.com/reaction/1729252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 14896448HCID 14896448—
SolventDichloromethaneHCID 6344—
ProductN-acetyl-N-(9-fluorenyl)-beta-alanin ethyl esterHCID 19011663—

Reaction Steps

0.51 mg of triethylamine and 0.28 ml of acetyl chloride were added under ice-cooling to a solution of 0.77 g of N-(9-fluorenyl)-β-alanine ethyl ester in 25 ml of methylene chloride. The resultant mixture was stirred at 0° C. for 0.5 hour and, then, at room temperature for 3 hours. The reaction solution was poured into ice-cold 1N hydrochloric acid and extracted with methylene chloride. The organic layer was washed with saturated sodium bicarbonate and saturated saline, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by a silica gel column chromatography (eluting solution: chloroform-methanol) to give 0.85 g of N-acetyl-N-(9-fluorenyl)-β-alanin ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332734
Source datasetuspto-grants-1994_07
ORD IDord-0d230d05ec934f549fab6617307721ad
Source noteuspto-grants-1994_07