HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(chloromethyl)-4-methyl-4H-1,2,4-triazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-methyl-4H-1,2,4-triazol-3-yl)methanol | HCID 15707893 | — |
| Product | 3-(chloromethyl)-4-methyl-4H-1,2,4-triazole hydrochloride | HCID 22381909 | — |
Reaction Steps
To thionyl chloride (2.0 ml) was added at 0° C. 3-hydroxymethyl-4-methyl-4H-1,2,4-triazole (0.15 g), and the mixture was refluxed for 1.5 hour. The reaction mixture was concentrated under reduced pressure, to which was added diethyl ether. Resulting crystals were collected by filtration and dissolved in ethanol, to which was added diethyl ether for recrystallization to afford 3-chloromethyl-4-methyl-4H-1,2,4-triazole hydrochloride (0.22 g) as colorless prisms, m.p. 96°-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405861 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-a3b94bad97f84c95a707606a77dcd282 |
| Source note | uspto-grants-1995_04 |