HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium cyanate → N-(4,5,6,7-Tetrahydro-1-benzothiophen-4-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | 4,5,6,7-Tetrahydrobenzo[b]thiophen-4-amine hydrochloride | HCID 17388600 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4,5,6,7-Tetrahydro-1-benzothiophen-4-yl)urea | HCID 13036998 | 22.1% |
Reaction Steps
A mixture of 50 grams of 4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine hydrochloride (about 45 grams real, based on 90% purity) in 100 ml. of water is stirred at about 15° C., and a solution of 23.1 grams of potassium cyanate in 100 ml. of water is added dropwise. After completion of the addition, the mixture is warmed slowly to 70° C. to 75° C. and held for an hour. The mixture is cooled, and the white solid is collected by filtration and washed with water. The solid is air-dried, pulverized, and washed with acetonitrile. On drying, this gives 37.3 grams of crude product, which on treatment with about 1200 ml. of hot acetone gives 11.45 grams, melting point 200° C. to 204° C. of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156670 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-5cc89ae9f10c461690698140f53193f9 |
| Source note | uspto-grants-1979_05 |