HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 6-Fluoro-7-benzyloxychroman-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-fluoro-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one | HCID 21186600 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-Fluoro-7-benzyloxychroman-4-one | HCID 21186590 | 73% |
Reaction Steps
A mixture of 6-fluoro-7-hydroxychroman-4-one (the compound of Preparation 29, 0.93 g, 5.11 mmol), benzyl bromide (0.61 mL, 5.13 mmol), potassium carbonate (1.41 g, 10.2 mmol) in acetone (100 mL) was stirred at ambient temperature overnight. The mixture was cooled, filtered, and concentrated to a yellow solid. This residue was recrystallized from ethyl acetate/ether to give 1.02 g (73%) of 6-fluoro-7-benzyloxychroman-4-one in two crops as cream white crystals which had: mp 155-156° C.; NMR δ7.58 (d, J=11 Hz, 1 H), 7.46-7.33 (m, 5 H), 6.54 (d, J=6.7 Hz, 1 H), 5.16 (d, 2 H), 4.50 (t, J=6.4 Hz, 2 H), 2.75 (t, J=6.4 Hz, 2 H). Analysis calculated for C16H13FO2: C, 70.58; H, 4.81. Found: C, 70.45; H, 4.80.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06258827B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6835b40a682e40d0a3c9b9a1b3ad3184 |
| Source note | uspto-grants-2001_07 |