HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-Methyl-N'-(4,5,6,7-tetrahydro-1-benzothiophen-4-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 4,5,6,7-Tetrahydrobenzo[b]thiophen-4-amine hydrochloride | HCID 17388600 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-Methyl-N'-(4,5,6,7-tetrahydro-1-benzothiophen-4-yl)urea | HCID 20348942 | — |
Reaction Steps
A mixture of 1.89 grams (0.01 mole) of 4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine hydrochloride in 20 ml. of dry benzene is stirred while 1.05 grams (0.01 mole) of triethylamine and 01.7 ml. (excess) of methyl isocyanate are added successively. Addition of the latter gives rise to an exotherm, and the mixture becomes very pasty. The mixture is kept at 45° C. for one hour, and after cooling to room temperature, the solid is collected, washed thoroughly with benzene and then with water. On drying, this gives 1.7 grams (81%) of product, melting point 183° C. to 186° C. Recrystallization from acetone gives 1.23 grams, melting point 187.5° C. to 189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156670 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-4f1f64d132c44aaeb9e82759444cf66b |
| Source note | uspto-grants-1979_05 |