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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271612Generated: October 26, 2026

(R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester → HCID 59834689, compound

https://huagongshe.com/reaction/271612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl esterHCID 8150601—
ReactantPotassium cyanateHCID 11378442—
SolventAcetic AcidHCID 176—
ProductHCID 59834689HCID 5983468989.3%

Reaction Steps

To a solution of 1.68 g (6.59 mmoles) of (R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester in 20 ml of acetic acid, 0.64 g (7.91 mmoles) of potassium cyanate is added at ambient temperature under N2 atmosphere. The mixture is stirred for 15 hours at ambient temperature and heated for 3 hours at 100° C., and then the reaction mixture is concentrated under reduced pressure. The mixture is extracted with AcOEt, and the combined extracts are washed with sat. NaHCO3 and brine, dried over MgSO4 and then concentrated under reduced pressure. The residue is purified by silica gel column chromatography to give 1.57 g of desired (R)-1-(4-chloro-benzyl)-5-isopropyl-imidazolidine-2,4-dione in 77% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452886B2
Source datasetuspto-grants-2008_11
ORD IDord-8d4fe44251374d84a781e4eb22e7633c
Source noteuspto-grants-2008_11