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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994281Generated: October 30, 2026

Sodium Hydroxide → 1-(Pentanoylamino)cyclopentane-1-carboxylic acid

https://huagongshe.com/reaction/1994281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantValeryl chlorideHCID 61186—
ReactantCycloleucine hydrochlorideHCID 3021985—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(Pentanoylamino)cyclopentane-1-carboxylic acidHCID 16726891—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 3 necked 250 ml round bottom flask equipped with mechanical stirrer, was charged with sodium hydroxide solution (24.1 g dissolved in 100 ml water) and 1-aminocyclopentane carboxylic acid hydrochloride (25 g) and chilled to 0° C. under stirring. Tetra butyl ammonium bromide (0.25 g) was added to the reaction mixture followed by slow addition of a solution of valeroyl chloride (27.5 g) in toluene (20 ml) during one hour at 0-5° C. under stirring. The reaction mass was stirred for 1 hour at 0-5° C. The reaction mixture was diluted with water (100 ml) toluene (20 ml) and stirred for 15 minutes. The two phases were separated. The aqueous phase was washed with toluene (20 ml). Aqueous phase was chilled to 10° C. and acidified with hydrochloric acid and stirred it for 1 hour. The product was filtered and washed with water. The product was dried at 60° C. till constant weight. (Yield: 22 g; 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652147B2
Source datasetuspto-grants-2010_01
ORD IDord-55cab2ef9d60477b972ce6cfefe1a5a6
Source noteuspto-grants-2010_01