HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Allylaminoacetaldehyde → HCID 20357128, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Allylaminoacetaldehyde | HCID 20548476 | — |
| Reactant | HCID 45077457 | HCID 45077457 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20357128 | HCID 20357128 | — |
Reaction Steps
6-Chlorobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-allylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about one hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-allyl-3-(6-chlorobenzothiazol-2-yl)ureido]acetaldehyde as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054574 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-e7f14269813540fe869111cde5a2905a |
| Source note | uspto-grants-1977_10 |