HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2-Bromoacetyl)-4-(4-ethylphenoxy)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(4-Ethylphenoxy)piperidine | HCID 13457429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Bromoacetyl)-4-(4-ethylphenoxy)piperidine | HCID 20283115 | 96.7% |
Reaction Steps
To a stirred suspension of 6.03 ml (69.3 mmol) of bromoacetyl bromide, 13.0 g (155 mmol) of sodium bicarbonate and 160 ml of dry dichloromethane in an ice bath was added dropwise a solution of 13.0 g (63.4 mmol) of 4-(4-ethylphenoxy)piperidine in 140 ml of dry dichloromethane. The mixture was stirred 1 hour at 0° and 45 minutes at room temperature. The mixture was subsequently poured into water, extracted twice with dichloromethane, washed with saturated sodium chloride and dried over potassium carbonate. Filtration followed by evaporation of the solvent provided 20.0 g (61.3 mmol) of 1-(2-bromoacetyl)-4-(4-ethylphenoxy)piperidine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518713 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-e42d91b4c432488c8cdb8b11af37204e |
| Source note | uspto-grants-1985_05 |