Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxypyridine | HCID 69278 | — |
| Reactant | Menthyl chloroformate | HCID 151928 | — |
| Reactant | HCID 178427853 | HCID 178427853 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86598850 | HCID 86598850 | — |
Reaction Steps
A solution of (−)-menthyl chloroformate (3.53 mL) in dry THF (15 mL) was added to a solution of 4-methoxypyridine (1.52 mL) in dry THF (35 mL) previously cooled to −78° C. under a nitrogen atmosphere. After 15 minutes, the solution containing the 4-fluoro-2-methyl-phenyl magnesium bromide was added drop-wise, and the mixture was stirred at −78° C. for 1 hour. The reaction was quenched by the addition of 1M hydrochloric acid solution (20 mL), warmed to r.t. and stirred at 23° C. for 30 minutes. After extraction with AcOEt (2×150 mL), the combined organic extracts were washed with brine (50 mL), dried and concentrated in vacuo to a residue, which was purified by flash chromatography (CH/THF/toluene 8:1:1) to give:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07648990B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-7d51999170544d5a8c123aaccf71f621 |
|---|
| Source note | uspto-grants-2010_01 |
|---|