HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22127020, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Ethyl 4-hydroxynaphthalene-2-carboxylate | HCID 13080945 | — |
| Product | HCID 22127020 | HCID 22127020 | — |
Reaction Steps
In an analogous manner to that described in Example 14(a), by alkylating ethyl 4-hydroxy-naphthalene-2-carboxylate [J. Agric. Chem Soc. Japan 24, 313 (1950)] with benzyl bromide there was obtained ethyl 4-benzyloxy-naphthalene-2-carboxylate as an almost colourless solid, Rf : 0.53 (SiO2, hexane:ethyl acetate=4:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150526 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-11de1ddcf0d747b0886ff6865e38bf95 |
| Source note | uspto-grants-2000_11 |