HuagongsheHuagongshe Chemistry Print Report · For research reference only
delta-Gluconolactone → 1-Naphthalenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | delta-Gluconolactone | HCID 7027 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Product | 1-Naphthalenemethanol | HCID 20908 | — |
Reaction Steps
As in Reaction Scheme 2, lithium-halogen exchange of compound (76), followed by addition of the resulting nascent lithiated aromatic to perbenzylated gluconolactone (2), produces a mixture of the corresponding lactols, which is reduced using triethylsilane and boron trifluoride etherate. Subsequent desilylation using tetrabutylammonium fluoride (TBAF) affords 1-naphthalenemethanol (77) in a reasonable yield for the three steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541380B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-bfedbb9e980745f9992a4ed0ae39d433 |
| Source note | uspto-grants-2013_09 |