HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178447560, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | Pivalic anhydride | HCID 15234 | — |
| Reactant | HCID 178447561 | HCID 178447561 | — |
| Reactant | HCID 178479701 | HCID 178479701 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178447560 | HCID 178447560 | — |
Reaction Steps
A mixture of 5.1 g. 4-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-benzotriazole hydrochloride, 6.7 g. pivalic anhydride and 33.3 g. molten pivalic acid is stirred for 3 days at ambient temperature, then poured on to ice, neutralized with an aqueous solution of ammonia and extracted with methylene chloride. After evaporation of the extract, the oily residue obtained is taken up in methanol and rendered weakly acidic with dilute hydrochloric acid. Upon evaporating the solvent, there are obtained 2.53 g. (38% of theory) 4-[2-pivaloyloxy-3-(4-phenoxymethylpiperidino)-propoxy]-benzotriazole hydrochloride; m.p. 131°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146630 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-8693d2e9261d49fb9c28452d0bf6d705 |
| Source note | uspto-grants-1979_03 |