HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 178419740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 178493079 | HCID 178493079 | — |
| Product | HCID 178419740 | HCID 178419740 | 78.6% |
Reaction Steps
A mixture of 8 gm (0.032 mol) of 2-(3,4,5-trimethoxy-phenylimino)-imidazolidine base and 150 ml of 48% of hydrobromic acid was refluced for 5 hours on an oil bath. Thereafter, the reaction mixture was evaporated in vacuo to half its original volume and allowed to stand overnight in the refrigerator. The amorphous precipitate which had formed was isolated and dried, yielding 7.3 gm (78.6% of theory) of 2-(3,4,5-trihydroxy-phenylimino)-imidazolidine hydrobromide, m.p. 204°-206° C., Rf -value 0.3 in mobile phase 75 parts sec.butanol, 15 parts formic acid, 10 parts water. Carrier: silicagel, visualization; potassium iodoplatinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250186 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-8266bc95747d43ea9da1c72cb45b8920 |
| Source note | uspto-grants-1981_02 |