HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(Chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (8-Fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol | HCID 66891073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(Chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxine | HCID 66889398 | 99.8% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of (8-fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol (0.84 g, 4.55 mmol) and triethylamine (960 μl, 4.84 mmol) in dichloromethane (20 mL) was slowly added thionyl chloride (400 μl, 5.47 mmol) at 0° C. The solution was stirred at 0° C. for 15 min then at rt for 3 h. Dichloromethane (80 mL) was added and the solution was washed with water (40 mL), saturated aqueous sodium bicarbonate (40 mL) then brine (40 mL) and dried over sodium sulfate. Filtration and concentration gave 7-(chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxine (0.92 g, quantitative yield) as a brown oil. The chloride was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872014B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-a09af8cc166b4f4b96e94c5d17242f8f |
| Source note | uspto-grants-2011_01 |