HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-Methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 6-Methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid | HCID 22571892 | 98% |
Reaction Steps
To a solution of methyl ether X (10.0 g, 60 mmol) in 50 ml THF at −78° C. was added n-butyllithium (36 ml, 90 mmol, 2.5 M in hexanes) was added drop-wise. After 1 h the solution was warmed to rt. After 1 h the solution was cooled to −78° C. and trimethyl borate (13.6 ml, 120 mmol) was added. The solution was warmed to rt. After 16 h the mixture was quenched by the addition of water and resulting mixture was acidified with AcOH and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, dried with MgSO4, filtered and concentrated in vacuo. The resulting oil was azeotroped with toluene to afford 6-methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid (13.72 g, 98%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008313B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-bc080b2e2c92426a83032e54ff395209 |
| Source note | uspto-grants-2011_08 |