Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225105Generated: October 26, 2026

5-Aminovaleric acid → 5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acid

https://huagongshe.com/reaction/225105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
Reactant2-(Chloromethyl)-4-methylvaleryl chlorideHCID 12769067—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acidHCID 20563967—

Reaction Conditions

Temperature5 °C

Reaction Steps

5-Aminovaleric acid (3.2 g) is dissolved in 15 ml of water containing 1.09 g of sodium hydroxide. This is cooled to 5° C. and 2-(chloromethyl)-4-methylvaleryl chloride in 30 ml of THF is added dropwise. The pH is maintained at 8-9 by the dropwise addition of 1.09 g sodium hydroxide in 20 ml of water as needed. After stirring for about 16 hours the reaction mixture is diluted with 30 ml of water and concentrated in vacuo to remove THF. The aqueous layer is washed with ether, and acidified with 10% hydrochloric acid. Product is extracted with ethyl acetate. The ethyl acetate is dried with magnesium sulfate, filtered and concentrated in vacuo to yield 4.3 g of product. Product is purified by the solvent system 500 parts ether: 10 parts methanol: 5 parts acetic acid, yielding 2.0 g of material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235885
Source datasetuspto-grants-1980_11
ORD IDord-77124c5d3e0744a2860c4d0810547d56
Source noteuspto-grants-1980_11