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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583672Generated: October 27, 2026

2-Chloro-N,N-dimethylethylamine → N-carbobenzyloxy-gamma-tert.butyl-L-glutamic acid-alpha-dimethylaminoethyl ester

https://huagongshe.com/reaction/1583672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantEthyl AcetateHCID 8857—
ReactantN-carbobenzyloxy-gamma-tert.butyl-L-glutamic acid-dicyclohexyl ammonium saltHCID 131714411—
SolventBenzeneHCID 241—
ProductN-carbobenzyloxy-gamma-tert.butyl-L-glutamic acid-alpha-dimethylaminoethyl esterHCID 5663388096.8%

Reaction Steps

To 28.2 g N-carbobenzyloxy-γ-tert.butyl-L-glutamic acid-dicyclohexyl ammonium salt, 360 ml ethyl acetate and 49.5 ml solution of dimethylaminoethylchloride in the amount of 11.7 g, which stoichiometrically corresponds to two times the molar volume, in benzene were added to be subjected to flux in oil bath at 90° C. for 16 hrs. After cooling, precipitated dicyclohexyl ammonium chloride was filtered off and ethyl acetate phase in the filtrate was washed with diluted hydrochloride to remove excessive dimethylaminoethylchloride contained therein. The filtrate was further washed with 10% aqueous solution of hydrogen sodium bicarbonate so as to remove the unreacted starting material and then with saturated brine to be neutral, which was then treated with sulfuric sodium anhydride for dehydration to be dried and subjected to reduced pressure distillation so as to distill off ethyl acetate and obtain the Intermediate I, N-carbobenzyloxy-γ-tert.butyl-L-glutamic acid-α-dimethylaminoethyl ester in the amount of 21.5 g (yield; 96.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552975
Source datasetuspto-grants-1985_11
ORD IDord-204a5bae281d4938ad35ce23883baedd
Source noteuspto-grants-1985_11