HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Chloro-5-formyl-2,3,6,7-tetrahydro-1H-azepine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Benzyl-4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-1-azepinecarboxylate | HCID 20481342 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Chloro-5-formyl-2,3,6,7-tetrahydro-1H-azepine hydrobromide | HCID 20481340 | — |
Reaction Steps
10.5 gm (0.036 mol) of benzyl 4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-1-azepine-carboxylate were mixed with 100 ml of a 40% solution of hydrogen bromide in glacial acetic acid, while stirring and cooling with ice. The mixture was then stirred for 3 hours at room temperature. It was then concentrated by evaporation in a rotary evaporator, and the residue was triturated with ether. After the ether had been decanted several times, the product was suction-filtered and washed twice with absolute ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414225 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-9eea466973144fb0a0aa34dc55483a3b |
| Source note | uspto-grants-1983_11 |