HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1,3,5-Trichloro-2-(chloromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,4,6-Trichlorobenzyl alcohol | HCID 4582574 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1,3,5-Trichloro-2-(chloromethyl)benzene | HCID 14939 | 100.2% |
Reaction Steps
To a stirred solution of 2,4,6-trichlorobenzylalcohol (10.0 g; 47.3 mmol) in chloroform (100 ml) kept under nitrogen atmosphere, thionyl chloride (6.07 ml; 85.1 mmol) was added slowly at 0° C. over a period of 15 minutes followed by catalytic amount of DMF. The reaction mix was allowed to stir at ambient temp for 3 hours. The reaction mixture was quenched with 50 ml of water; the aqueous layer was extracted with DCM (3×100 ml). The combined organic layer was washed with 5% sodium bicarbonate solution (2×50 ml) followed by brine (50 ml) and dried over anhydrous sodium sulphate. The solvent was evaporated under reduced pressure. 10.9 g (100% of theory) of 1,3,5-trichloro-2-chloromethyl-benzene was obtained in form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552049B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-a01f60e96bc24c12bb958b5b9a315755 |
| Source note | uspto-grants-2013_10 |