HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(2-Chlorophenyl)-3-(dimethylamino)propan-1-one--hydrogen chloride (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethanone, 1-(2-chlorophenyl)- | HCID 72864 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Chlorophenyl)-3-(dimethylamino)propan-1-one--hydrogen chloride (1/1) | HCID 24187272 | 61% |
Reaction Steps
At 0° C., concentrated HCl was added dropwise to Me2NH (40% in water, 5.57 mL, 1.1 equiv) to acidify the amine. After the addition, 1-(2-chlorophenyl)ethanone (6.18 g, 0.04 mol) and paraformaldehyde (1.68 g, 1.4 equiv) were added. The mixture was dissolved in ethanol (20 mL) and heated to reflux for 30 h. LC-MS found the starting material was gone. The reaction mixture was cooled to rt. The volatiles were removed in vacuo. EtOAc (30 mL) was added and the suspension was stirred for 15 min. The solid was collected by filtration and washed with EtOAc (2×5 mL). The white solid was dried under vacuum to afford 1-(2-chlorophenyl)-3-(dimethylamino)propan-1-one HCl salt (5.17 g, 61% yield). LC-MS (3 min) tR=0.72 min, m/z 212, 214(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598160B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-199801534e604fff9807cd213e92d7ce |
| Source note | uspto-grants-2013_12 |