HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethyl isocyanate → 1-(2-Chloroethyl)-3-(dicyclopropylmethyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | (Dicyclopropylmethyl)amine | HCID 83390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Chloroethyl)-3-(dicyclopropylmethyl)urea | HCID 98826 | — |
Reaction Steps
A solution made from 13.4 g of dicyclopropylmethylamine in 30 ml tetrahydrofuran is added dropwise to a solution of 13 g of β-chloroetyl isocyanate in 15 ml tetrahydrofuran while maintaining the inner temperature from 0° to +5° C. Then, the reaction mixture is kept at room temperature for 15 hours. Afterwards, the solution is evaporated to dryness and the dry residue, weighing 26.5 g, is used as such for the next step of the synthesis. For analytical purpose, a sample of the raw urea is recrystallised from acetonitrile. The N-(dicyclopropylmethyl) N-(β-chloroethyl) urea occurs as white crystals melting at 103°-104° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04102890 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-7e362a03602c4508823701aeddbc55a1 |
| Source note | uspto-grants-1978_07 |