HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,4,6-trimethyl-1H-indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,5,7-Trimethyl-1-indanone | HCID 11769049 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2,4,6-trimethyl-1H-indene | HCID 10920786 | 96% |
Reaction Steps
20.4 g (117 mmol) of 2,5,7-trimethyl-1-indanone (1) were dissolved in 300 ml of a mixture of tetrahydrofuran/methanol (2:1), and 6.6 g (175 mmol) of NaBH4 were added at room temperature. The mixture was stirred for a further hour, 50 ml of half-concentrated HCl were added and the mixture was extracted with ether. The combined organic phases were dried over sodium sulfate and freed from the solvent. The residue was transferred to a distillation apparatus, and 13 g of magnesium sulfate were added. A vacuum of about 10 mbar was applied and the mixture was heated up until the product distilled over (130-150° C.). Distillation gave 17.7 g of the indene 2 as a colorless oil. The yield was 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929264 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-a754499eed2841a8a0a23f48d6d3f3ef |
| Source note | uspto-grants-1999_07 |