HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873410Generated: October 26, 2026
Ammonia → 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]-5-methylselenophene
https://huagongshe.com/reaction/1873410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]selenophene | HCID 59456349 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]-5-methylselenophene | HCID 59456288 | — |
Reaction Steps
2.2 ml (13.0 mmol) of TMP are initially introduced at −15° C. in 15 ml of diethyl ether, and 8.2 ml (13.0 mmol, 15% soln. in hexane) of n-BuLi are metered in. After 25 min, a solution of 3.5 g (9.9 mmol) of 2-[4-(4-ethyl-cyclohexyl)-2,3-difluorophenyl]selenophene in 35 ml of diethyl ether is metered in at 0° C., and the mixture is stirred at RT for 2 h. The batch is cooled to −70° C., and 3.0 ml (48.2 mmol) of methyl iodide are added. The mixture is warmed to RT and stirred for 24 h. Sat. ammonium chloride soln. and conc. ammonia soln. are added successively, and the mixture is briefly stirred vigorously. The organic phase is separated off, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with 2 N hydrochloric acid and sat. sodium chloride soln. and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is purified by column chromatography (SiO2, n-heptane). The further purification is carried out by recrystallisation from ethanol. 2-[4-(4-Ethylcyclohexyl)-2,3-difluorophenyl]-5-methylselenophene is obtained as a solid having an m.p. of 63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304036B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-2e12a41be212405cb21f8be673ee3aba |
|---|
| Source note | uspto-grants-2012_11 |
|---|