HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(Chloromethyl)-1-fluoro-3-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Fluoro-6-methoxybenzyl alcohol | HCID 2779320 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(Chloromethyl)-1-fluoro-3-methoxybenzene | HCID 12979307 | — |
Reaction Steps
0.57 g (3.64 mmol) of 2-fluoro-6-methoxybenzyl alcohol was dissolved in 10 ml of benzene, and the resultant solution was added with 0.56 g (4.73 mmol) of thionyl chloride under a room temperature. The obtained solution was stirred for 1 hour at a room temperature to complete a reaction. The reacted solution was then condensed under reduced pressure to obtain a crude product of 2-fluoro-6-methoxybenzyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06589967B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-cda0b1b4a9ab46a195ed2b5f887a82e0 |
| Source note | uspto-grants-2003_07 |