HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (7-Fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 7-fluoro-2,3-dihydro-1,4-benzodioxine-5-carboxylate | HCID 49780160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-Fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanol | HCID 66891450 | 100% |
Reaction Steps
A solution of methyl 7-fluoro-2,3-dihydro-1,4-benzodioxine-5-carboxylate (400 mg, 1.88 mmol) in tetrahydrofuran (20 mL) was cooled to 0° C. and then added lithium aluminum hydride (3.78 mL, 1.0 M solution in tetrahydrofuran). The reaction mixture was allowed to warm to room temperature and stirred for 45 min, at which time water (143 μL) was added followed by 15% sodium hydroxide (143 μL) and then water (286 μL) again. The white precipitate was filtered and the filtrate was concentrated to give 345 mg (100%) of (7-fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanol as a colorless oil: 1H NMR (400 MHz, CDCl3): 6.63 (dd, J=2.8, 8.8 Hz, 1H), 6.56 (dd, J=3.2, 9.2 Hz, 1H), 4.64 (d, J=6.4 Hz, 2H), 4.28-4.25 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872014B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-bcc5e22d09ea44309364b0e3c64cfd25 |
| Source note | uspto-grants-2011_01 |