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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-bromo-2-oxocyclohexanecarboxylate | HCID 121765 | — |
| Reactant | [3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thiourea | HCID 71650841 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57780709 | HCID 57780709 | 87.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07923450B2 |
|---|
| Source dataset | uspto-grants-2011_04 |
|---|
| ORD ID | ord-aecc0193e8714b099597acf8daae22dc |
|---|
| Source note | uspto-grants-2011_04 |
|---|