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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377198Generated: November 1, 2026

Cesium fluoride → Methyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylate

https://huagongshe.com/reaction/2377198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
ReactantTolylboronic acidHCID 79799—
ReactantMethyl 4-benzyloxy-3-tert-butyl-5-iodobenzoateHCID 12084816—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylateHCID 1208481783%

Reaction Steps

12 g (28 mmol) of methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate are dissolved with 5.8 g (42 mmol) of 4-methylbenzeneboronic acid and 12.7 g (84 mmol) of caesium fluoride in 400 mL of dioxane. The reaction medium is degassed with a flow of nitrogen for 15 minutes, and 1.7 g (1.4 mmol) of tetrakis(triphenylphosphine)palladium are then added. The reaction medium is refluxed for 4 hours and then cooled and hydrolysed. After extraction with ethyl acetate, the organic phase is filtered and concentrated. The residue is purified by chromatography (eluent: 98 heptane/2 ethyl acetate): a colorless oil is obtained (m=9 g, yield=83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468457B2
Source datasetuspto-grants-2008_12
ORD IDord-085ac38486c845cb925cf3f08237060b
Source noteuspto-grants-2008_12