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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076015Generated: October 30, 2026

Ethyl 3-bromo-2-oxocyclohexanecarboxylate → HCID 57780709, compound

https://huagongshe.com/reaction/2076015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromo-2-oxocyclohexanecarboxylateHCID 121765—
Reactant[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
SolventEthanolHCID 702—
ProductHCID 57780709HCID 5778070987.3%

Reaction Steps

A suspension of [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea (131 mg, 0.50 mmol) and of 2-bromo-6-(carbethoxy)-cyclohexanone (137 mg, 0.55 mmol) in ethanol (5 mL) was stirred at room temperature for 2 days and then heated to reflux under an atmosphere of nitrogen over night. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel using dichloromethane/methanol (19:1 v/v) as eluent to yield the title compound (180 mg, 87%) as a white solid. MS ISP (m/e): 413.3 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=10.28 (s, 1H), 7.66 (d, 1H), 7.64 (s, 1H), 7.21 (d, 1H), 7.11 (d, 1H), 7.01 (s, 1H), 4.10 (q, 2H), 3.76 (s, 3H), 3.66 (m, 1H), 2.62 (m, 2H), 2.14 (s, 3H), 1.68-2.09 (m, 4H), 1.19 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923450B2
Source datasetuspto-grants-2011_04
ORD IDord-aecc0193e8714b099597acf8daae22dc
Source noteuspto-grants-2011_04