HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Tert-butyl 2-methylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 2-methylpropanoate | HCID 519334 | — |
Reaction Steps
To a solution of isobutyryl chloride (47 g, 0.44 mol) in CH2Cl2 (75 ml) and tert-butanol (75 ml) at 0° C., pyridine (39.3 ml, 486 mmol) was added slowly by syringe. The mixture was allowed to warm to room temperature, stirred overnight, diluted with CH2Cl2 (400 ml) and washed with H2O, HCl (2N, two times), H2O (two times) and saturated NaHCO3. The organic phase was dried over MgSO4 and filtered. The filtrate was then concentrated under reduced pressure without heat. The resulting oil was simply distilled, collecting the fraction boiling at 128-129° C. to give tert-butyl isobutyrate, 21 (35.9 g, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194448B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-ee2ca2f1cbae462582132114c9e9f5e7 |
| Source note | uspto-grants-2001_02 |