HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 12799743, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2,2-Dimethoxyethylmethylamine | HCID 8503 | — |
| Reactant | HCID 12799742 | HCID 12799742 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12799743 | HCID 12799743 | 94.2% |
Reaction Steps
At ambient temperatures, 5.4 grams (0.045 mole) of methylaminoacetaldehyde dimethylacetal was slowly added to a 50 milliliter benzene solution containing 8.4 grams (0.045 equivalents) of the 5-(1-methoxyethyl)-1,3,4-thiadiazol-2-yl isocyanate dimer (prepared above). The resulting solution was refluxed for 20 minutes; hexane was added resulting in the formation of an oil, the mixture was topped on a roto-vac at 70° C. to 13.2 grams of a hazy viscous oil which was dissolved in diethylether, and filtered. The diethylether solution was topped on a roto-vac at 70° C. to yield 12.9 grams of a red oil of 3-[5-(1-methoxyethyl)-1,3,4-thiadiazol-2-yl]-1-methyl-1-(2,2-dimethoxyethyl)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04314842 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-059a4bcc948c4f78a644c14703476fc8 |
| Source note | uspto-grants-1982_02 |