Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 15389070 | HCID 15389070 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | HCID 15389073 | HCID 15389073 | — |
Reaction Steps
760 mg (2.2 mmol) of methyl 2-hydroxy-4-[3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propynyl]benzoate and 20 ml of toluene are introduced into a three-necked flask under a stream of nitrogen. 4.4 ml of diisobutylaluminium hydride (1 M in toluene) are added at -78° C. and the mixture is allowed to return to room temperature. 9 ml of methanol and then 9 ml of hydrochloric acid (1 N) are successively introduced. The reaction medium is poured into an ethyl acetate/water mixture and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and then evaporated. The residue is purified by chromatography on a column of silica eluted with a mixture of ethyl acetate and heptane (50/50% by volume). After evaporation of the solvents, 200 mg (30%) of the expected alcohol are collected, with a melting point of 94-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06046220 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-2d2c295f6c8c4f89be3cdf7958cb58ad |
|---|
| Source note | uspto-grants-2000_04 |
|---|