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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461215Generated: November 3, 2026

Pyridine → ethyl gamma-(N-carbobenzoxy)amino-gamma-cyanobutanoate

https://huagongshe.com/reaction/1461215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 131716763HCID 131716763—
SolventTetrahydrofuranHCID 8028—
Productethyl gamma-(N-carbobenzoxy)amino-gamma-cyanobutanoateHCID 5372534379.5%

Reaction Steps

To a suspension of 21.45 g of N-carbobenzoxy-carbonyl-L-isoglutamine ethyl ester in 200 mL of dry tetrahydrofuran kept at 0° C. to -5° C. in an ice-bath 11.82 mL of pyridine is added. To the above solution 9.84 mL of trifluoroacetic anhydride in 100 mL of tetrahydrofuran is added dropwise at such a rate that the bath temperature is maintained. The solution is stirred for 2 hours at this temperature. The solution is evaporated to dryness and the oil is dissolved in ethyl acetate. The organic layer is washed with 1.0 N hydrochloric acid and sterile water. The solution is dried and evaporated in vacuo to give an oil to give 14.8 g of ethyl γ-(N-carbobenzoxy)amino-γ-cyanobutanoate, 17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075099
Source datasetuspto-grants-1991_12
ORD IDord-4a91d5da208e48aaaa6f65c31e612057
Source noteuspto-grants-1991_12