HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → [3,4-Dimethoxy-2-(methoxymethyl)phenyl]boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Bromo-3,4-dimethoxy-2-(methoxymethoxy)benzene | HCID 86677573 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | [3,4-Dimethoxy-2-(methoxymethyl)phenyl]boronic acid | HCID 67462911 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a stirring solution of 1-bromo-3,4-dimethoxy-2-methoxymethoxy-benzene (1 g, 3.62 mmol) in tetrahydrofuran (15 mL) at −78° C., was added n-butyllithium (5.5 mL, 7.24 mmol) and stirred for 20 min to this trimethylborate (3.76 g, 36.23 mmol) was added and the resultant reaction mixture was stirred for 30 min at −78° C. The reaction mixture was quenched with saturated ammonium chloride solution and extracted with ethyl acetate (3×). The combined ethyl acetate layer was washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford 3,4-dimethoxy-2-(methoxymethyl)phenylboronic acid as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051290B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-d9cd85bb11fb41b6881b1ca274ea02e3 |
| Source note | uspto-grants-2015_06 |