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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-carbobenzyloxy-gamma-tert.butyl-L-glutamic acid-dicyclohexyl ammonium salt | HCID 131714411 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-carbobenzyloxy-gamma-tert.butyl-L-glutamic acid-alpha-dimethylaminoethyl ester | HCID 56633880 | 96.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04552975 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-204a5bae281d4938ad35ce23883baedd |
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| Source note | uspto-grants-1985_11 |
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