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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644731Generated: October 25, 2026

1,2-Dichloroethane → [6-Fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1644731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl pent-3-ynoateHCID 13378967—
Reactant4-Fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehydeHCID 59350830—
CatalystGold tribromideHCID 82525—
SolventHexaneHCID 8058—
Product[6-Fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl esterHCID 593508023.1%

Reaction Steps

To a mixture of 4-fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehyde (example 2-1, 3rd step) (2.02 g, 6.68 mmol) and pent-3-ynoic acid methyl ester (3.03 g, 26.8 mmol) in 1,2-dichloroethane (40 mL), was added gold(III) bromide (0.264 g, 1.18 mmol). The resulting mixture was heated at 80° C. for 2 hours before additional gold(III) bromide (0.125 g, 0.59 mmol) was added. Another portion of gold(III) bromide (0.125 g, 0.59 mmol) was added after 2 more hours. After a total of 6 hours of heating, the reaction mixture was cooled to room temperature, and the solvent was removed to afford a brown oil. Flash chromatography (Aspire FlashReady™, 50 μm, 30% ethyl acetate in hexane) gave [6-fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester (87 mg, 3.1%). HRMS (ESI+) cald. for C22H19FO5S [(M+Na)+] 437.0829, obsd. 437.0827.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124629B2
Source datasetuspto-grants-2012_02
ORD IDord-c959dbfcb8bc4d81aa034a9c6ecddd3f
Source noteuspto-grants-2012_02