HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-[1-beta-Chloroethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 5-Bromothiazol-2-yl Isocyanate | HCID 23062264 | — |
| Reactant | 2-beta-Chloroethylaminoacetaldehyde | HCID 54332049 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-[1-beta-Chloroethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde | HCID 54185255 | — |
Reaction Steps
5-Bromothiazol-2-yl isocyanate dimer (17.0 grams), benzene (70 ml) and the dimethyl acetal of 2-β-chloroethylaminoacetaldehyde (13.5 grams) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is then stirred at room temperature for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent under reduced pressure, leaving an oil. This oil is dissolved in an ethanol-water mixture, and the solution is filtered. The filtrate is then stripped of solvents under vacuum to yield the desired product the dimethyl acetal of 2-[1-β-chloroethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118390 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-e9d1dbcfe0cb4b728f59227f01ab5eca |
| Source note | uspto-grants-1978_10 |