HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indene-1-carboxylic acid, 2,3-dihydro- → 1-Indanmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indene-1-carboxylic acid, 2,3-dihydro- | HCID 85728 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Indanmethanol | HCID 271880 | 74.4% |
Reaction Steps
To a suspension of LiAlH4 (4.7 g) in diethyl ether (200 ml) was added dropwise a solution of AlCl3 in diethyl ether (200 ml). A solution of 1-indanecarboxylic acid (10 g) (prepared according to the method of Hansen et al. Helv. Chim. Acta 1982, 33, 325-343) in dry tetrahydrofuran (200 ml) was added drop-wise at 10-15° C. The mixture was finally stirred at room temperature for 1.5 hours. Excess AlH3 was destroyed by addition of concentrated aqueous NaOH solution (25 ml) at 0° C. Precipitated inorganic salts were filtered off and the solvents evaporated in vacuo leaving 6.8 g of the title compound 1a as a viscous oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262087B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-5160c76122754528949ce56e6f311607 |
| Source note | uspto-grants-2001_07 |