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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249963Generated: October 30, 2026

Methyl Acrylate → HCID 20716712, compound

https://huagongshe.com/reaction/1249963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant6-Bromo-2-naphthalenolHCID 27144—
ReactantTri-o-tolylphosphineHCID 80271—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
ProductHCID 20716712HCID 2071671271.4%

Reaction Steps

5 g (22.4 mmol) of 6-bromo-2-naphthol, 6 ml (67.2 mmol) of methyl acrylate, 100 mg (0.45 mmol) of palladium acetate and 25 ml of triethylamine were placed in a flask gassed with nitrogen. After the addition of 545 mg (1.79 mmol) of tri-(o-tolyl)-phosphine the reaction mixture was boiled under reflux overnight. After 15 hours the reaction was interrupted and the mixture was partitioned between ethyl acetate and water. The organic phase was back-washed three times with water and the aqueous phases were each individually back-washed twice with ethyl acetate. The combined organic phases were dried over magnesium sulphate, filtered over Celite and evaporated completely in a vacuum. Chromatography on silica gel with toluene/ethyl acetate (3:2) and subsequent recrystallization from ethyl acetate gave 3.65 g of methyl (E)-3-(6-hydroxy-naphthalen-2-yl)-acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335409B1
Source datasetuspto-grants-2002_01
ORD IDord-3f0d9c9fd4274b8390b6bb3d6b884440
Source noteuspto-grants-2002_01