HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515697Generated: October 28, 2026
Thionyl Chloride → 4-(Chloromethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzene
https://huagongshe.com/reaction/515697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-(Cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanol | HCID 67211680 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Chloromethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzene | HCID 67249147 | 100% |
Reaction Steps
To a solution of (4-(cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanol (0.060 g, 0.220 mmol) in toluene (2 mL) was added thionyl chloride (1.32 mmol). The reaction was heated to 75° C. for 3 h and quenched with water at 0° C. The mixture was extracted with hexanes (twice). The combined organics were washed with saturated NaHCO3(aq), dried over MgSO4, and concentrated to give the title compound as an oil (0.220 mmol). 1H NMR (400 MHz, CDCl3) δ ppm 0.91-1.06 (m, 2H), 1.12-1.23 (m, 3H), 1.61-1.74 (m, 6H), 2.66 (d, J=6.95 Hz, 2H), 4.59 (s, 2H), 7.30 (d, J=7.96 Hz, 1H), 7.47 (d, J=7.96 Hz, 1H), 7.63 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09108969B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-897cc3b67f094b319fa856663e0df3f8 |
|---|
| Source note | uspto-grants-2015_08 |
|---|