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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261825Generated: November 3, 2026

Hydrochloric Acid → 3-Butoxy-4'-hydroxy-2'-methyl-biphenyl-4-carbaldehyde

https://huagongshe.com/reaction/2261825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantSodium CarbonateHCID 10340—
Reactant3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 57443272—
Reactant4-Bromo-2-butoxy-benzaldehydeHCID 57443341—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product3-Butoxy-4'-hydroxy-2'-methyl-biphenyl-4-carbaldehydeHCID 8663546985.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenol (0.210 g, 0.898 mmol) and 4-bromo-2-butoxy-benzaldehyde (0.210 g, 0.817 mmol) in 1,4-dioxane (20 mL) is evacuated and re-filled with N2 3 times. To this solution, Pd(PPh3)4 (0.010 g) and aqueous Na2CO3 (1.0 mL, 2.0 M) are added. The resulting mixture is heated at 90° C. for 24 hours under N2. The reaction mixture is cooled to room temperature, neutralized with HCl (1.0 M, 3.0 mL), and concentrated. The residue is extracted with ethyl acetate (30 mL×2), and the combined organic layers are dried over sodium sulfate and concentrated. The residue is purified via silica gel chromatography eluting with 25-30% ethyl acetate in hexanes to give the title compound (0.198 g, 85%). ES/MS m/e 283.0 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-2d30b2296a224fcf8de33c6e0dbd0753
Source noteuspto-grants-2010_12