HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → Methyl 6-(4-hydroxyphenyl)-1-naphthoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| Reactant | Methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoate | HCID 22622428 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 6-(4-hydroxyphenyl)-1-naphthoate | HCID 59264867 | 88.3% |
Reaction Steps
A solution of methyl 6-{[(trifluoromethyl)sulfonyl]oxy}-1-naphthoate (271 g, 0.81 mol) (from multiple batches), tetrakis(triphenylphospine)palladium (0) (37.4 g, 0.032 mol), 2 M sodium carbonate solution (1.3 L) and 4-hydroxyphenyl boronic acid (134 g, 0.97 mol) in ethylene glycol dimethyl ether (1.5 L) was heated at 80° C. for 1.5 h. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (2 L) and water (2 L). The ethyl acetate layer was dried over anhydrous sodium sulfate, filtered and concentrated to a dark semisolid residue. The crude material was purified by crystallization from dichloromethane-heptane to give 199 g of the product as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705028B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-382534a3568140809b5caf4f4d95c772 |
| Source note | uspto-grants-2010_04 |