HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 19098304, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 19098302 | HCID 19098302 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19098304 | HCID 19098304 | — |
Reaction Steps
The desired compound is prepared by subjecting 2-(N-carbobenzyloxy-glycylimino)-3-methyl-1,3,4-thiadiazoline-5-sulphonamide (0.5 gm) suspended in glacial acetic acid (5ml) to a solution of hydrogen bromide in glacial acetic acid (32% w/w. 8.0 ml) at room temperature for about 1 hour with stirring. Diethyl ether (50 ml) is then added and the mixture set aside for three hours at 0° C. The solid precipitate is collected, washed with diethyl ether, and dried to give the desired product, 2-(glycylimino)-3-methyl-1,3,4-thiadiazoline-5-sulphonamide hydrobromide, m.p. 209°-210° C. (0.4 gm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288735 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-5695bd4e776042699bebcd000ce4d90a |
| Source note | uspto-grants-1994_02 |