HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-(chloromethyl)-3-t-butyl-1H-1,2,4-triazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-t-butyl-1H-1,2,4-triazole1-ylmethanol | HCID 57712418 | — |
| Product | 1-(chloromethyl)-3-t-butyl-1H-1,2,4-triazole hydrochloride | HCID 23149120 | — |
Reaction Steps
The mixture of 1.38 g of 3-t-butyl-1H-1,2,4-triazole1-ylmethanol and 2.7 ml of thionyl chloride was stirred under reflux condition for 3 hours. After the reaction mixture was cooled to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was recrystallized from hexane to obtain 1.72 g of 3-t-butyl-1-(chloromethyl)-1H-1,2,4-triazole hydrochloride. 1H-NMR (CDCl3, TMS, δ (ppm)): 1.36 (9H, s), 5.83 (2H, s), 8.17 (1H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541374B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-0233433b0e7c40e2b7795291e72393a0 |
| Source note | uspto-grants-2009_06 |