HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → 7-Methoxy-2-(tetrahydrofuran-2-yl)-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1-(7-Methoxybenzofuran-2-yl)-butane-1,4-diol | HCID 18423647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Methoxy-2-(tetrahydrofuran-2-yl)-benzofuran | HCID 18423638 | 71.3% |
Reaction Steps
A solution of 1-(7-methoxybenzofuran-2-yl)-butane-1,4-diol (0.88 g) was treated with p-toluenesulfonic acid monohydrate (10 mg) and 3 Å molecular sieves in dichloromethane (10 ml) at ambient temperature. After stirring for 1 hour the solvent was removed in vacuo. The residue was purified by column chromatography on silica eluting with 20% ethyl acetate in hexane to give the title compound as a yellow oil (0.58 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455561B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-eb973e94b9224c61b7066eccc23f5b70 |
| Source note | uspto-grants-2002_09 |