HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[(8-cyclohexyloctyl)amino]-N-3-bromopropylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromopropan-1-amine hydrobromide | HCID 12570703 | — |
| Reactant | p-(8-Cyclohexyloctyl)aminobenzoyl chloride hydrochloride | HCID 20475769 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-[(8-cyclohexyloctyl)amino]-N-3-bromopropylbenzamide | HCID 20475775 | — |
Reaction Steps
To a slurry of 21.80 g. of 2-bromopropylamine hydrobromide in 200 ml. of glyme at 3° C. is added a solution of 23.96 g. of 4-(8-cyclohexyloctylamino)benzoyl chloride hydrochloride in 65 ml. of glyme, concurrently with 26 ml. of triethylamine diluted to 39 ml. with glyme. The solution is warmed to reflux and 0.2 g. of 4-dimethylaminopyridine is added. The solution is heated for four hours and cooled overnight. The solid is removed by filtration and the filtrate diluted with 200 ml. of water. The precipitate is collected and crystallized from cyclohexane. The solid is recrystallized from acetonitrile to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04227014 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-8ebd1c9ca8684c6ab92b724d97ae688f |
| Source note | uspto-grants-1980_10 |