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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443315Generated: November 1, 2026

Valeryl chloride → N-((2'-Cyano(1,1'-biphenyl)-4-yl)methyl)-N-(1-oxopentyl)-L-valine methyl ester

https://huagongshe.com/reaction/1443315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantValeryl chlorideHCID 61186—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2'-Cyanobiphenyl-4-ylmethyl)-L-valine Methyl Ester HydrochlorideHCID 16744793—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-((2'-Cyano(1,1'-biphenyl)-4-yl)methyl)-N-(1-oxopentyl)-L-valine methyl esterHCID 16744795107.7%

Reaction Conditions

Temperature28 °C

Reaction Steps

150 g N-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine methyl ester hydrochloride was charged into a round bottomed flask containing a mixture of sodium bicarbonate (158.1 g), water (450 ml) and toluene (900 ml). The contents were stirred at 28° C. for 25 minutes and then cooled to 0° C. 110.9 g of valeryl chloride was added slowly to the reaction mass at 0-20° C. over about 55 minutes. The reaction mass was stirred at about 2-4° C. for about 2 hours. Reaction completion was confirmed by thin layer chromatography and the reaction mixture was allowed to attain 28° C. 450 ml of water was added to the reaction mass and stirred for about 20 minutes. The organic layer was separated, washed with a solution of sodium bicarbonate (30 g) in water (450 ml) twice, followed by washing with water (450 ml). The organic layer was concentrated under reduced pressure at 60-68° C. to obtain 183 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659406B2
Source datasetuspto-grants-2010_02
ORD IDord-9abacb88bd514a0fb0a6d8a5e8aba653
Source noteuspto-grants-2010_02