HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Indanone → HCID 19047540, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Indanone | HCID 6735 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19047540 | HCID 19047540 | 104% |
Reaction Steps
To a solution of 2.7 mL (0.027 mol) of 10M n-butyllithium in hexane in 70 mL of ether cooled to -78° C. was added 4 g (0.027 mol) of 3-bromofuran and the mixture was stirred for 15 min. To the above cooled mixture was added 3.17 g (0.024 mol) of indanone in 10 mL of THF and the mixture was allowed to warm to room temperature, and then stirred for 20 min. To the mixture was added saturated ammonium chloride solution and the resulting mixture was extracted with ethyl acetate (3×100 mL), and the organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo to afford 5 g of crude 1-(3-furyl)-indan-1-ol, as an orange oil, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554620 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-33fc585ebb3c4d0fba59bd5c2a3f9fc5 |
| Source note | uspto-grants-1996_09 |