HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 1-Benzyl 4-chloro-2,3,6,7-tetrahydro-5-oximinomethylene-1H-azepine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-benzyl-5-chloro-2,3,6,7-tetrahydro-1H-azepine-4-carbaldehyde hydrochloride | HCID 18943541 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzyl 4-chloro-2,3,6,7-tetrahydro-5-oximinomethylene-1H-azepine hydrochloride | HCID 86739108 | — |
Reaction Steps
45 gm (0.16 mol) of 1-benzyl-4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-azepine hydrochloride were suspended in 450 ml of ethyl alcohol, and at 30° C. 12.2 gm (0.175 mol) of hydroxylamine hydrochloride were added in batches while stirring. After some hours, a crystalline precipitate separated out of the gradually clearing solution. The reaction mixture was stirred for 2 hours more and then allowed to stand overnight. The crystalline precipitate was suction-filtered off and dried. After evaporation of the mother liquor, another 10 gm were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414225 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-5fb27cbf32a543e3a9e3ceb9efe7c1c7 |
| Source note | uspto-grants-1983_11 |