HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470487Generated: October 30, 2026
Potassium Phosphate, Tribasic → 1-Methoxy-5-methylnaphthalene
https://huagongshe.com/reaction/1470487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Methylboronic Acid | HCID 139377 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 5-Methoxynaphthalen-1-yl trifluoromethanesulfonate | HCID 11066726 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 1-Methoxy-5-methylnaphthalene | HCID 10975953 | 88.8% |
Reaction Steps
In a 500 mL 2-neck round bottom flask, toluene (300 mL) and deionized water (14 mL) were added and degassed under nitrogen for 20 minutes. Then, 5-methoxynaphthalen-1-yl trifluoromethanesulfonate (above Step-2 intermediate) (14 g, 45.75 mmol) was added to the above mixture. After stirring for 10 min at RT, K3PO4 (34 g, 160 mmol) and methylboronic acid (4.1 g, 68.6 mmol) were added followed by Pd(OAc)2 (1.03 g, 4.6 mmol) and BINAP (5.7 g, 9.15 mmol) and the reaction mixture was stirred at RT for 15 min under nitrogen and then heated to 100° C. overnight. It was cooled and diluted with saturated NH4Cl solution (150 mL). The aqueous layer was extracted with EtOAc (4×100 mL) and the combined organic layer was washed with water (100 mL), brine (100 mL), dried and filtered. After solvent removal, the crude product obtained was purified by column chromatography (5% EtOAc:Hexanes) to yield the desired compound (7 g, 87%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006442B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-3c01cd9ab524490eb81a81603ffbe48d |
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| Source note | uspto-grants-2015_04 |
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