HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethoxyethylmethylamine → HCID 13021504, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethoxyethylmethylamine | HCID 8503 | — |
| Reactant | HCID 53747785 | HCID 53747785 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13021504 | HCID 13021504 | — |
Reaction Steps
4.9 grams (0.036 mole) of methylaminoacetaldehyde dimethylacetal was slowly added to a warm 30 milliliter benzene solution containing 10.2 grams (0.036 mole) of the 5-[1-(3-chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanate dimer (prepared above). The resulting solution was refluxed for 15 minutes, cooled, topped on a roto-vac at 70° C. to 14.5 grams of a pink solid residue which was recrystallized from a minimum amount of ethylacetate/hexane solution. The fluffy precipitate was filtered off, and dried in a vacuum oven at 80° C. to 10.3 grams of fluffy white crystals of 3-[5-[1-(3-chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl]-1-methyl-1-(2,2-dimethoxyethyl)urea. Melting point 127°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04269983 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-164592ed444345ff8175283faa2ecb05 |
| Source note | uspto-grants-1981_05 |