HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Pivaloylamino)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Pivaloylamino)pyridine | HCID 1051519 | — |
Reaction Steps
To a solution of 94.1 g (1.0 mol) of 2-aminopyridine and 173 ml (1.25 mol) of triethylamine in 400 ml of dichloromethane were added dropwise, whilst cooling with ice water, 132.5 g (1.099 mol) of pivaloyl chloride in 150 ml of dichloromethane. The. mixture was stirred for 2 hours at room temperature and filtered to remove the triethylamine hydrochloride formed. The filtrate was washed with water and twice with 5% aqueous sodium hydrogen carbonate solution, then dried over sodium sulphate. After working up in the usual way 157.5 g (88.4% of theory) of colourless crystals of melting point 74-76° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498325B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-ff6a90c0b5fb4cd7861aa8294d016af9 |
| Source note | uspto-grants-2009_03 |