HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 1-Indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 4-Hydroxy-1-indanone | HCID 590547 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Indanone | HCID 6735 | 79.9% |
Reaction Steps
To a solution of 4-hydroxy-1-indanone (25.0 g, 169 mmol) and imidazole (28.7 g, 422 mmol) in DMF (500 ml) was added tert-butyldimethylchiorosilane. The reaction mixture was stirred overnight at room temperature and treated with water (500 ml) and extracted with diethyl ether (500 ml). The organic phase was collected and dried over sodium sulfate. Evaporation gave a yellow oil which was distilled under reduced pressure to give indanone (1) (35.44 g, 135 mmol, 79.9%) as a colourless oil (120–121° C./0.1 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074863B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-c27413ba3f90416cbba4e2a1548bf543 |
| Source note | uspto-grants-2006_07 |