HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 10878919, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 86585221 | HCID 86585221 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10878919 | HCID 10878919 | — |
Reaction Steps
A suspension consisting of 60 g of azobisisobutyronitrile, 28 g of methanol and 270 ml of toluene was reacted by introducing 32 g of hydrogen chloride to obtain a toluene suspension of 2,2′-azobis(1-imino-1-methoxy-2-methylpropane) hydrochloride. The toluene suspension was neutralized with ammonia, followed by filtering to obtain a toluene solution of 2,2′-azobis(1-imino-1-methoxy-2-methylpropane). To the toluene solution was added 62 g of pyrrolidine, and reacted for 7 hours. After standing overnight, ethyl acetate was poured into the reaction solution, and crystals ware filtered and dried to obtain 10 g of pale yellow crystal of 2,2′-azobis [2-methyl-1-(N-pyrrolidinyl)iminopropane].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403774B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-108e1fad27274ca5971c3b816ba67158 |
| Source note | uspto-grants-2002_06 |