HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → (5-Fluoro-2,3-dihydro-1-benzofuran-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Allyl-4-fluorophenol | HCID 11344112 | — |
| Product | (5-Fluoro-2,3-dihydro-1-benzofuran-2-yl)methanol | HCID 19886355 | 57.7% |
| Product | HCID 58566367 | HCID 58566367 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To an ice cold solution of 2-allyl-4-fluorophenol (853) (6.0 g, 36.2 mmol) in CHCl3 (180.0 mL) was added slowly the suspension of 77% 3-chloroperoxybenzoic acid (8.1 g, 36.2 mmol) in CHCl3 (36.2 mL). The resulting mixture was stirred at 0° C. for 2 hours, then washed with NaHCO3 (100 mL), water (2×100 mL), brine (100 mL) and dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (30-40% EtOAc in hexanes) to provide the desired product (5-fluoro-2,3-dihydrobenzofuran-2-yl)methanol (854) (3.8 g, 57.7%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476308B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-cdf474847c30401cbe6888681cf2c38d |
| Source note | uspto-grants-2013_07 |