HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester → HCID 59834689, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester | HCID 8150601 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59834689 | HCID 59834689 | 89.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452886B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-8d4fe44251374d84a781e4eb22e7633c |
| Source note | uspto-grants-2008_11 |