HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Buten-2-ol → HCID 54483366, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | 5,6-Dimethoxy-1-indanone | HCID 75018 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 2,2-Dimethoxypropane | HCID 6495 | — |
| Product | HCID 54483366 | HCID 54483366 | 27% |
Reaction Steps
A solution of 20 g of 5,6-dimethoxy-1-indanone, 21.5 ml (0.25 mol) of 3-buten-2-ol and 200 mg of p-toluenesulfonic acid in 21.5 ml of 2,2-dimethoxypropane and 200 ml of anhydrous toluene was boiled under reflux for 24 hours. The reaction mixture was subsequently concentrated in a vacuum and purified by column chromatography on silica gel (hexane/ethyl acetate 3:2). 6.8 g (27%) of (RS)-2-(2-buten-1-yl)-5,6-dimethoxy-1-indanone were obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646173 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-50b761c09df744ab872e07e9b17024c5 |
| Source note | uspto-grants-1997_07 |