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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethylboronic AcidHCID 139377—
ReactantBinap, (A+-)-HCID 634876—
Reactant5-Methoxynaphthalen-1-yl trifluoromethanesulfonateHCID 11066726—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAmmonium ChlorideHCID 25517—
Product1-Methoxy-5-methylnaphthaleneHCID 1097595388.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006442B2
Source datasetuspto-grants-2015_04
ORD IDord-3c01cd9ab524490eb81a81603ffbe48d
Source noteuspto-grants-2015_04