HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(Chloromethyl)-1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | {1-[4-(Pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazol-5-yl}methanol | HCID 86691877 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(Chloromethyl)-1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazole | HCID 86691879 | — |
Reaction Steps
Thionyl chloride (1.72 g, 14.4 mmol) was added to a stirred solution of {1-[4-(pentafluoro-λ6-sulfanyl)phenyl]-1H-tetrazol-5-yl}methanol (Intermediate 44, 3.50 g, 11.6 mmol) in toluene (40 mL), SOCl2 at room temperature. The reaction mixture was stirred for 4 hr at reflux. The reaction mixture was concentrated under vacuum. The residue was diluted with DCM and washed with ice-water, saturated aq NaHCO3 and brine solution, dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the crude compound. This was purified by column chromatography (100-200 mesh silica gel), eluted with 20%-30% EtOAc/pet-ether to give the title compound as a brown gum (3.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115132B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-f7aa9686189d4119b57558a68359dcb3 |
| Source note | uspto-grants-2015_08 |