HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3-Dihydro-5-nitrospiro[benzofuran-2,4'-piperidine]hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3-Dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine] | HCID 12733235 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3-Dihydro-5-nitrospiro[benzofuran-2,4'-piperidine]hydrochloride | HCID 20394271 | — |
Reaction Steps
A solution of 3.4 g of 2,3-dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine] in 150 ml of 6 N hydrochloric acid is refluxed for 45 hours and then stirred at ambient temperature for 16 hours. Thereafter, the reaction mixture is successively extracted once with ether, basified with 6 N sodium hydroxide and extracted thrice with ether. The combined ether extracts are dried and the solvent removed, leaving a yellow residue. The residue is dissolved in ether where it is converted to its hydrogen chloride salt. The salt is collected, dried and finally recrystallized twice from ethyl alcohol to give the product 2,3-dihydro-5-nitrospiro[benzofuran-2,4'-piperidine]hydrochloride, mp 265°-266° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166120 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-122d54bf01484a2792bd4ac12456da3a |
| Source note | uspto-grants-1979_08 |