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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289306Generated: October 31, 2026

Toluene → Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oate

https://huagongshe.com/reaction/1289306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 6-bromonaphthalene-2-carboxylateHCID 1249959—
Reactant(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acidHCID 22571498—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
SolventSodium CarbonateHCID 10340—
ProductEthyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oateHCID 22571563—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a degassed solution of 0.39 g (1.4 mmol) of ethyl 6-bromonaphthalene-2-carboxylate and 3.0 mL of toluene, was added sequentially 49 mg (0.04 mmol) of tetrakis-triphenylphosphine palladium(0), 2.0 mL (2.0 mmol) of 1M sodium carbonate and then a solution of 0.32 g (1.6 mmol) of (5,6,7,8-tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid (Compound B13) in 3.0 mL of MeOH. The reaction was heated at 80° C. for 6 h, diluted with 2N Na2CO3, and extracted with CH2Cl2 (2 x), the organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Flash chromatography (silica, 5% ethyl acetate in hexane) of the crude material gave the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747542
Source datasetuspto-grants-1998_05
ORD IDord-4d23b2bb8990472a86339d8efc69e885
Source noteuspto-grants-1998_05