HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 20300309, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methyl-2-sulfanylideneimidazolidine-4,5-dione | HCID 20300326 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20300309 | HCID 20300309 | 46% |
Reaction Steps
Triethylamine (84 ml, 0.60 mole) was added dropwise over a period of 6 hours to a stirred solution of 1-methyl-2-thioxo-4,5-imidazolidinedione (88 g, 0.61 mole) and 1,5-dibromopentane (264 g, 1.20 mole) in dimethylsulphoxide (650 ml) at room temperature. The mixture was allowed to stand overnight and then poured into ice water (3 liters) containing concentrated hydrobromic acid (1 ml). The mixture was extracted with chloroform and the extracts were washed with water, dried over magnesium sulphate and evaporated to give an oil which was treated with hexane to give yellow crystals of 1-(5-bromopentyl)-3-methyl-2-thioxo-4,5-imidazolidinedione (82.3 g), m.p. 48°-50°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04084001 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-4c3c951bf6054e4bba261877c0f3890d |
| Source note | uspto-grants-1978_04 |