HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-Buten-2-one, 4-(2,3-dihydro-1H-inden-5-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Indanecarboxaldehyde | HCID 121624 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Buten-2-one, 4-(2,3-dihydro-1H-inden-5-yl)- | HCID 4073927 | 81% |
Reaction Steps
An aqueous solution of 10% sodium hydroxide (50-70 ml) was added dropwise over a period of 5 minutes to a suspension of indane-5-carboxaldehyde (18.50 g; 127 mmole) in acetone (50 ml) and water (50 ml). The mixture was stirred at a temperature of 65° C. for a period of 11/2 hours and then extracted with dichloromethane (200 ml). The organic extract was washed several times with water, dried over anhydrous sodium sulphate, and the solvent was removed under reduced pressure using a rotary evaporator to give 1-(5-indanyl)but-1-en-3-one (19.25 g; 81%) as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110989 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-bb8f46a3df0542a6981a9802cbb25294 |
| Source note | uspto-grants-1992_05 |