HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Chloromethyl)-2-fluoro-1-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (3-Fluoro-4-methylphenyl)methanol | HCID 2774590 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(Chloromethyl)-2-fluoro-1-methylbenzene | HCID 18624147 | — |
Reaction Steps
Thionyl chloride (0.892 g, 7.5 mmol) was added to a solution of the product of STEP 1 (1.0 g, 6.4 mmol) in 10 ml ether dropwise at 0° C. After 30 min, the reaction was quenched with crushed ice carefully, and diluted with H2O. The product was extracted with ether. The organic layer was washed with saturated NaHCO3 solution, brine, dried with Na2SO4, and concentrated. The residue was purified by chromatography (on silica gel, ethyl acetate/hexane=1/9) to give a colorless liquid in 10.5 g. NMR spectra of the product were consistent for the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531494B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-ecf6119a27da40c481bd79cb57489a5c |
| Source note | uspto-grants-2003_03 |