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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277353Generated: November 3, 2026

Ethyl Acetate → HCID 12807303, compound

https://huagongshe.com/reaction/1277353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-L-ValineHCID 83693—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 12807303HCID 1280730389.2%

Reaction Steps

1 liter of ethyl acetate was added to 80 g of BOC-Val.DCHA and the mixture was washed twice with 600 ml of sulfuric acid and water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain the free acidin an oily form. The free acid and 28 g of H-Gly-OEt.HCl were dissolved in a solvent mixture of 150 ml of chloroform and 150 ml of THF. The solution was cooled and 28 ml of triethylamine and 41.2 g of DCC were added thereto. The resultant mixture was stirred at a temperature of 0° to -2° C. for 1 hour and at room temperature overnight. The insoluble materials were removed by filtration and the filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate, washed with 1 N hydrochloric acid, water, a 5% sodium bicarbonate aqueous solution and water, dried over magnesium sulfate and concentrated in vacuo. The resulting residue was crystallized by addition of n-hexane and recrystallized from ethyl acetate-diethyl ether-n-hexane to obtain 54 g (89.2%) of the desired material with a melting point of 94°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277393
Source datasetuspto-grants-1981_07
ORD IDord-4db5c50d0d1149369e3378b6889c7402
Source noteuspto-grants-1981_07