HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367356Generated: October 26, 2026
Hydrochloric Acid → 2-Amino-1-(3-chlorophenyl)ethanone
https://huagongshe.com/reaction/2367356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 2-Bromo-3'-chloroacetophenone | HCID 38738 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 2-Amino-1-(3-chlorophenyl)ethanone | HCID 3026272 | 239.4% |
Reaction Steps
2-Bromo-1-(3-chlorophenyl)ethanone (2.0 g, 8.57 mmol) was added to a solution of hexamethylenetetramine (1.201 g, 8.57 mmol) in CHCl3 (60 mL), and the resulting mixture was heated at 55° C. for 1 hour. The mixture was cooled to room temperature, and the white precipitate was collected by filtration, washed with CHCl3, and dried in vacuo to afford 3.1 g. This white solid was suspended in a mixture of ethanol (50 mL) and hydrochloric acid (0.25 mL, 8.30 mmol) and heated at 105° C. for 1.5 hours. The mixture was cooled to 0° C., filtered and washed by ethanol (30 mL). The organic phase was concentrated to afford an HCl salt of the title compound (1.74 g) as a pale yellow solid. LC-MS (ES) m/z=170 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08697685B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-da34b2e5395648f4a39a9abfc3c65137 |
|---|
| Source note | uspto-grants-2014_04 |
|---|