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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl pent-3-ynoate | HCID 13378967 | — |
| Reactant | 4-Fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehyde | HCID 59350830 | — |
| Catalyst | Gold tribromide | HCID 82525 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | [6-Fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester | HCID 59350802 | 3.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124629B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-c959dbfcb8bc4d81aa034a9c6ecddd3f |
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| Source note | uspto-grants-2012_02 |
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