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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361786Generated: October 30, 2026

Ethanol → HCID 14104007, compound

https://huagongshe.com/reaction/361786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Cyclohexyl-L-alanineHCID 712421—
ProductHCID 14104007HCID 14104007—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-[N-[N-(4-(piperidin-4-yl)butanoyl)-N-ethylglycyl]aspartyl]-L-β-cyclohexyl alanine, ethyl ester ##STR16##A. β-cyclohexyl alanine (1.5 g) is dissolved in absolute ethanol (75 ml) and the solution cooled to 0° C. Thionyl chloride (1.1 ml) is added dropwise over a period of 10-15 minutes, the solution allowed to warm to room temperature, and then stirred at room temperature for about 18 hours. The reaction mixture is evaporated in vacuo, toluene is azeotroped twice from the residue, and the residue is taken up into ethyl acetate. The ethyl acetate solution is washed with water, 1N sodium hydroxide, water, brine, dried over sodium sulfate, filtered, and evaporated in vacuo to give β-cyclohexyl alanine, ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866685
Source datasetuspto-grants-1999_02
ORD IDord-e6b6d140ba56458f94527d369b13dbad
Source noteuspto-grants-1999_02