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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583117Generated: November 3, 2026

Triethylamine → HCID 20728730, compound

https://huagongshe.com/reaction/1583117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 20728729HCID 20728729—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20728730HCID 2072873084.3%

Reaction Steps

A mixture of 2-methoxycarbonylmethyl-6-trifluoromethanesulfonyloxy-benzoic acid methyl ester (2.705 g, 7.6 mmol), LiCl (2.355 g, 55.6 mmol), NEt3 (1.5 mL, 10.8 mmol), Pd[P(C6H5)3]4(1.09 g, 0.94 mmol), and tributyl (vinyl)tin (2.85 mL, 9.75 mmol) in dioxane (50 mL) was heated at reflux. After 3 h, the reaction was allowed to cool to rt, filtered through a pad of silica gel and concentrated. The crude product was purified by flash chromatography on SiO2(13% EtOAc/hexanes) to afford 2-methoxycarbonylmethyl-6-vinyl-benzoic acid methyl ester as a yellow solid (1.50 g, 84%): 1H NMR (CDCl3) δ3.67 (s, 3H), 3.89 (s, 5H), 5.32 (d, J=10.9 Hz, 1H), 5.68 (d, J=17.4 Hz, 1H), 6.82 (dd, J=17.4, 10.9 Hz, 1H), 7.20 (d, J=7.1 Hz, 1H), 7.36 (m, 1H), 7.50 (d, J=7.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740777B2
Source datasetuspto-grants-2004_05
ORD IDord-f49052ff75e84f538082080e358dfeec
Source noteuspto-grants-2004_05