HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Bromo-2-methyl-1-(4-piperidinophenyl)-propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 2-Methyl-1-(4-(piperidin-1-yl)phenyl)propan-1-one | HCID 21257191 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-2-methyl-1-(4-piperidinophenyl)-propan-1-one | HCID 19879519 | — |
Reaction Steps
34.70 g (0.15 mol) of 2-methyl-1-(4-piperidinophenyl)-propan-1-one are dissolved in 200 ml of glacial acetic acid. 0.58 g (5.0 mmol) of chlorosulfonic acid (corresponding to 0.33 ml) are added as catalyst. 24.0 g (0.15 mol) of bromine are then added dropwise at room temperature with thorough stirring in the course of approximately one hour. The solution is then poured onto ice and is brought to about pH 6 with dilute sodium hydroxide solution. The precipitated crystals are extracted with toluene. The toluene solution is dried with Na2SO4 and is concentrated at 40° C. under the vacuum of a rotary evaporator. The slowly crystallising, orange liquid is then reacted further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05145885 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-15b40a3a8d1641dcb358cdf3e5abae03 |
| Source note | uspto-grants-1992_09 |