HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333946Generated: October 26, 2026
Sodium Hydroxide → HCID 66835573, compound
https://huagongshe.com/reaction/333946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-2,2-difluoroacetaldehyde | HCID 93560 | — |
| Reactant | 2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanone | HCID 86691595 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66835573 | HCID 66835573 | 10% |
| Product | (E)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one | HCID 66835852 | 7% |
Reaction Steps
2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanone (78.3 mg, 0.2 mmol) was dissolved in anhydrous THF (1 ml), NaH was added (12 mg of a 60% dispersion in mineral oil, 0.3 mmol) and the mixture was stirred for 30 minutes at room temperature. 2-Chloro-2,2-difluoro-acetaldehyde (0.3 mmol, the solution of step D) was added, the temperature was raised to 45° C. and stirring was continued for 3 hours. The mixture was diluted with water, basified with 0.1 NaOH and extracted with diethylether (2×). The combined organic phases were washed with 5% sodium bicarbonate solution, water, dried over magnesium sulfate and the solvent was removed under reduced pressure. The raw product was purified by preparative HPLC (gradient of water containing 0.1% ammonia and acetonitrile) to yield (E)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (5 mg, 0.014 mmol, 7%) and (Z)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (7 mg, 0.02 mmol, 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08883791B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-4c1d92d7f5d24620a11bc1003c227871 |
|---|
| Source note | uspto-grants-2014_11 |
|---|