HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-bromopropyl)-2-(4-tetradecenylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | 2-(4-Tetradecenylamino)benzoyl chloride hydrochloride | HCID 73708085 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | N-(3-bromopropyl)-2-(4-tetradecenylamino)benzamide | HCID 54261894 | — |
Reaction Steps
To a slurry of 21.80 g. of 3-bromopropylamine hydrobromide in 200 ml. of glyme at 3° C. is added a solution of 23.9 g. of 2-(4-tetradecenylamino)benzoyl chloride hydrochloride in 65 ml. of glyme, concurrently with 26 ml. of triethylamine diluted to 39 ml. with 1,2-dimethoxyethane. 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 and the mother liquor diluted with 200 ml. of water to yield a solid which is crystallized from cyclohexane and recrystallized from acetonitrile to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440940 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-edc8f3b061ed4b3995aa791cd60751cd |
| Source note | uspto-grants-1984_04 |