HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Ethyl 5-Benzyloxy-3-hydroxy-2-naphthoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 3,5-dihydroxynaphthalene-2-carboxylate | HCID 14773083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-Benzyloxy-3-hydroxy-2-naphthoate | HCID 14773084 | 7% |
Reaction Steps
To a stirred solution of 7.8 g (0.34 g atom) of sodium in 1,000 cc of ethanol, was added 85 g (0.37 mole) of ethyl 3,5-dihydroxy-2-naphthoate. After one-half hour 47 g (0.37 mole) of benzyl chloride was added. The reaction mixture was warmed under reflux for 24 hours. The hot reaction mixture was filtered and cooled in an ice bath. A tan solid precipitated out, which was filtered off yielding 15.0 g (m.p. 98°-115° C.) of the crude product. Recrystallization first from ethanol and then from acetonitrile furnished ethyl 5-benzyloxy-3-hydroxy-2-naphthoate, m.p. 112°-114° C. in 7 percent yield (7.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015663 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-191deefae9934f7f92c4754152a056ec |
| Source note | uspto-grants-1991_05 |