HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749466Generated: November 4, 2026
Thionyl Chloride → 1-(Chloromethyl)-4-fluoro-2-methylbenzene
https://huagongshe.com/reaction/749466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Fluoro-2-methylphenyl)methanol | HCID 3872017 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Chloromethyl)-4-fluoro-2-methylbenzene | HCID 20511816 | 100% |
Reaction Steps
(4-Fluoro-2-methylphenyl)methanol (11.5 g, 82 mmol) was dissolved in CH2Cl2 (100 mL). The mixture was cooled to 0° C. before adding SOCl2 (10.7 g, 90 mmol), then stirred for 30 min at 0° C. and then at room temperature for 1.5 h. The solvent and excess of SOCl2 were removed by evaporation followed by the addition of CH2Cl2. The solvent and remaining traces of SOCl2 were evaporated once more. There was obtained 13.0 g (100%) of 1-(chloromethyl)-4-fluoro-2-methylbenzene as an oil. 1H NMR (300 MHz, CDCl3): 2.4 (s, 3H), 4.6 (s, 2H), 6.8-7.0 (m, 2H), 7.3 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07402581B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-e4780ea8b04548c3aacbdfe22a6d5b38 |
|---|
| Source note | uspto-grants-2008_07 |
|---|