HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isocyanate → (5-Bromo-4-methylpyridin-2-yl)-n-t-butyl carboxylic amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isocyanate | HCID 62412 | — |
| Reactant | 2,5-Dibromo-4-methylpyridine | HCID 2734429 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (5-Bromo-4-methylpyridin-2-yl)-n-t-butyl carboxylic amide | HCID 68468634 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
2,5-Dibromo-4-methylpyridine (1.83 g, 7.29 mmol) was dissolved in toluene (100 mL), cooled to −78° C. and a solution of nBuLi (4.4 mL, 8.8 mmol, 2.0 M in pentane) was added dropwise and stirred at −78° C. for 2 h. A solution of tBuNCO (1.1 mL, 9.5 mmol) in toluene (3 mL) was added dropwise and stirred for 1 h at −78° C. then warmed to −10° C. and quenched by addition of NH4Cl (aq). After warming to r.t. the reaction was extracted with ether and the organics dried over Na2SO4 and concentrated. The product was used without further purification. MS [M+H]+: 271.0; tR=2.44 min. (method 1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952161B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-a2a4e62c06ae4a3ab68047fc7d2d9ef3 |
| Source note | uspto-grants-2015_02 |