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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261821Generated: October 30, 2026

Hydrochloric Acid → HCID 67529691, compound

https://huagongshe.com/reaction/2261821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-fluoro-benzoic acid methyl esterHCID 11345311—
Reactant3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 57443272—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67529691HCID 6752969179%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenol (0.241 g, 1.03 mmol) and 4-bromo-2-fluoro-benzoic acid methyl ester (0.240 g, 1.03 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 and 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 (0.211 g, 79%). 1H NMR (400 MHz, CDCl3): δ 7.95-7.91 (t, 1H), 7.10-7.04 (m, 3H), 6.74-6.69 (m, 2H), 3.93 (s, 3H), 2.21 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-da453fc20e4b4002afb5f058ca03cdc2
Source noteuspto-grants-2010_12