Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430592Generated: October 31, 2026

tert-Butanol → HCID 86671521, compound

https://huagongshe.com/reaction/1430592

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantPotassium thiocyanateHCID 516872—
ReactantHCID 66786996HCID 66786996—
SolventWaterHCID 962—
ProductHCID 86671521HCID 8667152194.3%

Reaction Steps

200 g (0.758 mol) 4-Cyclohexylamino-3-oxo-butyric acid ethyl ester hydrochloride were dissolved in 360 ml water and 120 ml tert-butanol and were heated to 90° C. Then 88.4 g (0.91 mol) KSCN were added and the mixture was heated for 20 s, thereby a phase separation occurred. After cooling to RT, the phases were separated and the aqueous layer was extracted with AcOEt. The combined organic layers were washed with Brine, dried with MgSO4 and concentrated. The solid was digested in MTBE and filtered to yield 192 g (0.715 mol, 94%) of (1-Cyclohexyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester as a beige solid. HPLC: tR=1.16 min (YMC J′ sphere ODS H 80 20×2.1 mm, 4 μm, A: H2O+0.05% TFA, B: MeCN, 4%→95% B in 2 min, 1 ml/min, 30° C.); Mass (ES+) (C13H20N2O2S): calculated. 268. found 269 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940901B2
Source datasetuspto-grants-2015_01
ORD IDord-4bcf9c977d0b4fc4846db837fcf1d44f
Source noteuspto-grants-2015_01