HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(3,3-Dimethyl-2,3-dihydrobenzofuran-5-yl-oxysulfonyl)-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Dimethyl-2,3-dihydro-1-benzofuran-5-ol | HCID 22401450 | — |
| Reactant | HCID 178527437 | HCID 178527437 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3,3-Dimethyl-2,3-dihydrobenzofuran-5-yl-oxysulfonyl)-1,2,4-triazole | HCID 178428843 | — |
Reaction Steps
5.4 g of 3,3-dimethyl-5-hydroxy-2,3-dihydrobenzofuran was dissolved in 30 ml of tetrahydrofuran, and then 4.6 ml of triethylamine was added while stirring the solution. Then, 5.0 g of 3-chlorosulfonyl-1,2,4-triazole was gradually added while cooling with ice and stirring the solution. Then, this was stirred for 14 hours. Tetrahydrofuran was evaporated, and 2N hydrochloric acid was added and extracted with ethyl acetate. The organic layer was washed with brine, dried with magnesium sulfate, and the solvent was removed, so that coarse crystals were obtained. This was then recrystallized from n-hexane/ethyl acetate, so that 2.7 g of the titled compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05527818 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-b48b170192124475be4619b0ef856e34 |
| Source note | uspto-grants-1996_06 |