HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-Allyloxy-3-fluoro-4-chloromethyl-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Allyloxy-2-fluoro-phenyl)-methanol | HCID 69292836 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Allyloxy-3-fluoro-4-chloromethyl-benzene | HCID 69293378 | 97% |
Reaction Steps
A solution of 4.20 g (23.1 mmol) (4-allyloxy-2-fluoro-phenyl)-methanol in 80 ml dichloro-methane and 0.5 ml DMF was cooled to 0° C. 2.17 ml (3.57 g, 30.0 mmol) thionyl chloride were added slowly and then stirred for 1 h at room temperature. Dichloromethane was distilled off. The residue was taken up in 100 ml ethyl acetate and washed with concentrated sodium carbonate solution. The organic phase was dried and evaporated to give 4.47 g (97%) 1-allyloxy-3-fluoro-4-chloromethyl-benzene as colored oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432291B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-3e1914b6e5b347aab30dda1f8f095043 |
| Source note | uspto-grants-2008_10 |