HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-(2,3-Dihydro-1H-inden-5-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Indane | HCID 10326 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2,3-Dihydro-1H-inden-5-yl)ethan-1-one | HCID 233976 | — |
Reaction Steps
A mixture of indane (1, 12.25 mL, 0.10 mol) and Ac2O (11.34 mL, 0.12 mol) was added dropwise for 1 h to a slurry of AlCl3 (26.7 g, 0.2 mol) in DCM (100 mL) at 0° C. The reaction mixture was warmed up to room temperature and stirred for 15 h. The mixture was cooled to 0° C. and quenched by slow addition of water (20˜30 mL) and 1M HCl (50 mL). The organic layer was separated, washed with brine and saturated NaHCO3 solution, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude product 2 was dried under high vacuum and used without further purification (16.1 g, 0.10 mol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034921B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-7cb499739c72469d816bb696f28f45b6 |
| Source note | uspto-grants-2015_05 |