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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249264Generated: October 31, 2026

Ethyl alpha-oxobenzenebutanoate → HCID 13749507, compound

https://huagongshe.com/reaction/1249264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18605807HCID 18605807—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 13749507HCID 13749507—

Reaction Steps

Dissolve 422 mg of 3-(S)-amino-1-(1-carboxyethyl)perhydroazepin-2-one hydrochloride in water and adjust the pH to 6.8 with 2M tetrabutylammonium hydroxide. Lyophilize the solution and dissolve the residue in 10 ml absolute ethanol. Add 1.98 g ethyl 2-oxo-4-phenylbutyrate and 7 g. powdered 4A molecular sieves. Add a solution of 357 mg. sodium cyanoborohydride in 3 ml absolute ethanol at a rate of 0.5 ml/hour. After the addition is complete, stir the reaction mixture overnight at room temperature. Filter the reaction mixture, wash the filter cake with ethanol and concentrate the combined filtrate and washings at aspirator pressure. Dissolve the residue in water and add 20 ml ether and 20 ml Dowex 50 (H+). Stir the mixture for 1 hour then draw off the ether layer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04629787
Source datasetuspto-grants-1986_12
ORD IDord-86233636b8094f34aeb7e1e13be8299b
Source noteuspto-grants-1986_12