HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982072Generated: October 30, 2026
Methyl 9-bromononanoate → HCID 15725722, compound
https://huagongshe.com/reaction/982072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 9-bromononanoate | HCID 554142 | — |
| Reactant | HCID 19982286 | HCID 19982286 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 15725722 | HCID 15725722 | 202.3% |
Reaction Steps
Sodium hydride (588 mg of a 60% dispersion in mineral oil, 13 mmol) was washed twice with hexane and covered with dimethylformamide (DMF), (45 mL). 3,3,5-Triphenyl-3H-pyrazole (3 g, 10 mmol) was added and the mixture stirred at 110° C. under a nitrogen atmosphere for 30 minutes before being cooled to room temperature. Methyl 9-bromononanoate (2.80 g, 11 mmol) in DMF (2 mL) was added dropwise, the mixture stirred at room temperature for 2 hours and then poured onto water (100 mL). The mixture was extracted with diethyl ether (3×100 mL), the extracts washed with water (3×100 mL), dried over sodium sulfate and concentrated to give an oil. Chromatography on a column of silica gel using a mixture of hexane and diethyl ether (2:1) as eluent afforded methyl 3,4,5-triphenyl-lH-pyrazol-1-nonanoate (4.72 g, 100%) as a viscous oil. (MS(CI): m/e =467 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04994482 |
|---|
| Source dataset | uspto-grants-1991_02 |
|---|
| ORD ID | ord-156272ed273a4a6287c57ddb30c7521c |
|---|
| Source note | uspto-grants-1991_02 |
|---|