HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-(Chloromethyl)-4-phenylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Phenylthiophen-2-yl)methanol | HCID 12941349 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(Chloromethyl)-4-phenylthiophene | HCID 58306635 | — |
Reaction Steps
4-Phenyl thiophene-2-methanol (0.21 g), toluene (2.0 mL), and a catalytic amount of pyridine were added, and thionyl chloride (0.16 mL) was added dropwise thereto under ice-cooling. After stirring at room temperature for 3 hours, the reaction mixture was concentrated under reduced pressure, azeotroped with toluene, and dried at 60° C. under reduced pressure to obtain 2-(chloromethyl)-4-phenylthiophene (0.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598355B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-4e3358ab301a4978a0f11c11dcb5fe3c |
| Source note | uspto-grants-2013_12 |