HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminum hydride → {3-[2-(Methyloxy)ethyl]-1-naphthalenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 3-[2-(methyloxy)ethyl]-1-naphthalenecarboxylate | HCID 66896973 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | {3-[2-(Methyloxy)ethyl]-1-naphthalenyl}methanol | HCID 66895342 | — |
Reaction Steps
Methyl 3-[2-(methyloxy)ethyl]-1-naphthalenecarboxylate (1 eq.) from the previous step was taken up in toluene (0.1 M). To this solution was then added DIBAl-H (1.5 M toluene solution, 2.4 eq.) and the resulting solution was vigorously stirred at RT for 4 h. The reaction mixture thus obtained was quenched with 1 N aq. HCl and extracted with ether. The combined organic extracts were washed further with water and brine, dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo afforded the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889714B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-349d526a99cd44dd8403205221475222 |
| Source note | uspto-grants-2014_11 |