HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylethanolamine → Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride (1:1) | HCID 13054189 | — |
Reaction Steps
A solution of N-benzyl-2-aminoethanol (12, 79.05 g, 0.523 mole) in chloroform (400 niL) was treated with thionyl chloride (80 mL, 1.09 mole) at room temperature. The resulting mixture was heated to reflux (6 h). The solvent was removed in vacuo, the residue dissloved in hot ethanol (1.3 L) and cooled overnight. The solids were collected via suction filtration and dried in vacuo at 65° C. (24 h) to afford the title compound 13 as white plates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922722 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-f06f7d0bd63041069f897055c7083c2e |
| Source note | uspto-grants-1999_07 |