HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydro-1-benzofuran-7-carboxylic acid → (2,3-Dihydro-1-benzofuran-7-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydro-1-benzofuran-7-carboxylic acid | HCID 2795014 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2,3-Dihydro-1-benzofuran-7-yl)methanol | HCID 2795020 | 77.3% |
Reaction Steps
Added BH3 (1M in THF, 9 mL) to a solution of 2,3-dihydro-1-benzofuran-7-carboxylic acid (481 mg, 2.93 mmol) in THF (7 mL) drop wise at 0° C., thereto, the mixture was stirred at room temperature overnight. Extracted with ethyl acetate twice, and washed the organic phase with brine and dried with anhydrous Na2SO4, concentrated to give the title compound (340 mg, 77%). 1H NMR (400 MHz, CDCl3): δ 2.09 (1H, s), 3.22 (2H, t, J=8.8 Hz), 4.61 (2H, t, J=8.8 Hz), 4.67 (2H, s), 6.83 (1H, t, J=7.6 Hz), 7.08 (1H, d, J=7.2 Hz), 7.14 (1H, d, J=7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987461B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c7896538a4f948978dcaf7195f04c336 |
| Source note | uspto-grants-2015_03 |