HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20301130, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12577035 | HCID 12577035 | — |
| Reactant | HCID 19889661 | HCID 19889661 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20301130 | HCID 20301130 | — |
Reaction Steps
With continuous stirring and cooling, 4.1 g of α-(chlorothio)-isobutyronitrile are added dropwise at 0° to 10° C. to a solution of 6.97 g of 2-[1-(2,3-dimethylphenoxy)-propyl]-2-imidazoline of the formula ##STR4## and 4 g of triethylamine in 80 ml of toluene. The reaction mixture is stirred for 1 hour at room temperature, then the toluene phase is washed repeatedly with water and dried. The toluene is then evaporated off, affording 1-(2-cyano-prop-2-ylthio)-2-[1-(2,3-dimethylphenoxy)-propyl]-2-imidazoline of the formula ##STR5## in the form of a yellow viscous oil with a melting point of 58°-60° C. The following compounds of the formula I can be obtained by procedures analogous to the one described in this Example: ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04241075 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-101d9c26c1644426a92171d2e2d7bdcf |
| Source note | uspto-grants-1980_12 |