HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Pivaloyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(5-bromo-6-methyl-pyridin-2-yl)-2,2-dimethyl-propionamide | HCID 960161 | — |
| Product | Pivaloyl chloride | HCID 62493 | — |
| Product | 2-Pyridinamine, 5-bromo-6-methyl- | HCID 170678 | — |
Reaction Steps
This material was prepared in analogy to example 107 step A] from N-(5-bromo-6-methyl-pyridin-2-yl)-2,2-dimethyl-propionamide, 7.05 g—obtained via standard acylation of 5-bromo-6-methyl-pyridin-2-ylamine with 2,2-dimethyl-propionyl chloride in CH2Cl2, with triethylamine as base, as viscous brown oil, MS (ESI): 271.2 (MH+)- butyllithium (34.94 mL, 1.6 M in hexane, Agros) and N,N-dimethylformamide (4 mL) as an amorphous light brown solid (5.7 g). MS (EI): 220.1 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482341B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-9e3036ef1df1419cb73606988cb1c783 |
| Source note | uspto-grants-2009_01 |