HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(Decyloxy)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid → HCID 23297274, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(Decyloxy)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 18960121 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23297274 | HCID 23297274 | 94.9% |
Reaction Steps
0.34 g (8.95 mmol) of lithium aluminum hydride was added to 40 ml of ether. To this mixture was slowly added 2.54 g (7.65 mmol) of the 6-decyloxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid obtained in the first stage of Example 1. After the resulting mixture was stirred at room temperature for 30 minutes, it was heated under reflux for 6 hours. After cooling, the reaction mixture was caused to undergo hydrolysis and extraction with ether. The organic phase was concentrated and by purifying the concentrate using column chromatography there was obtained 2.31 g (7.26 mmol) of 6-decyloxy-1,2,3,4-tetrahydro-2-hydroxymethylnaphthalene as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117359 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-877250b1befc4293a5f6a8fe3ca5e3d9 |
| Source note | uspto-grants-2000_09 |