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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427871Generated: November 2, 2026

Sodium Carbonate → Tert-butyl 4-(adamantan-1-ylmethoxy)-fluoro-5-vinylbenzoate

https://huagongshe.com/reaction/1427871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
ReactantTributyl phosphine tetrafluoroborateHCID 71317416—
ReactantTert-butyl 4-(adamantan-1-ylmethoxy)-5-chloro-2-fluorobenzoateHCID 86702858—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 4-(adamantan-1-ylmethoxy)-fluoro-5-vinylbenzoateHCID 86702895—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 4-(adamantan-1-ylmethoxy)-5-chloro-2-fluorobenzoate (2.00 g, 5.06 mmol), vinylboronic acid pinacol ester (1.56 g, 10.1 mmol) and sodium carbonate (1.61 g, 15.2 mmol) in dioxane (20 mL) and water (5 mL) was bubbled with a nitrogen atmosphere for 10 min, tributylphosphine tetrafluoroborate (0.15 g, 0.51 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.023 g, 0.025 mmol) was added to this reaction mixture. The reaction mixture was heated to 100° C. for 24 h and then cooled to ambient temperature. Water (50 mL) was added and the mixture extracted with ethyl acetate (100 mL×3), the combined organics were washed with brine; dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified over column chromatography, eluting with 30% dichloromethane in hexanes to give the crude product, which was used for next step without further purification: MS (ES+) m/z 398.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933236B2
Source datasetuspto-grants-2015_01
ORD IDord-3d58a6dd81a64e7793603905a081e44f
Source noteuspto-grants-2015_01