HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → 2-methyl-7-(2,4,6-trimethyl-phenyl)-3-vinyl-2H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1-[2-methyl-7-(2,4,6-trimethyl-phenyl)-2H-indazol-3-yl]-ethanol | HCID 59702285 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-methyl-7-(2,4,6-trimethyl-phenyl)-3-vinyl-2H-indazole | HCID 59702345 | 55% |
Reaction Steps
A solution of 1-[2-methyl-7-(2,4,6-trimethyl-phenyl)-2H-indazol-3-yl]-ethanol (0.263 g, 0.893 mmol) and 4-toluenesulfonic acid hydrate (0.217 g, 1.14 mmol) in 10 mL of toluene was stirred at 103° C. for 16 h then allowed to cool. The yellow-orange solution was sequentially washed with 10 mL of a 10% aqueous NaOH solution and 10 mL of a saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated to an orange oil. Column chromatography (20% EtOAc/hexanes) afforded 2-methyl-7-(2,4,6-trimethyl-phenyl)-3-vinyl-2H-indazole (15: Ra=Rb=H, Ar=2,4,6-trimethylphenyl; 0.135 g; 55%; m.p. 84.9-95.4) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365211B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-b172ceb4c6424a74af9bb016fbb0c39c |
| Source note | uspto-grants-2008_04 |