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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427476Generated: November 1, 2026

4-Methoxycarbonylphenylboronic acid → 3',5'-Dichloro-4'-(1-oxo-2-aza-spiro[4.5]dec-2-ylmethyl)-biphenyl-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2427476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxycarbonylphenylboronic acidHCID 2734369—
Reactant2-(4-Bromo-2,6-dichloro-benzyl)-2-aza-spiro[4.5]decan-1-oneHCID 24863746—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product3',5'-Dichloro-4'-(1-oxo-2-aza-spiro[4.5]dec-2-ylmethyl)-biphenyl-4-carboxylic acid methyl esterHCID 2486374864%

Reaction Conditions

Temperature90 °C

Reaction Steps

Purge with N2 a mixture of 2-(4-bromo-2,6-dichloro-benzyl)-2-aza-spiro[4.5]decan-1-one (0.14 g, 0.36 mmol) and 4-methoxycarbonyl phenylboronic acid (0.19 g, 1.05 mmol) in toluene (10 mL) and 2M sodium carbonate (1.25 mL). Treat the reaction with Pd(PPh3)4 (0.041 g, 0.035 mmol) and heat to 90° C. for 4 hours under N2. Cool the reaction and dilute with ethyl acetate, and then wash with 1N HCl and water. Dry the organic layer with Na2SO4 and remove the solvent in vacuo to afford crude product. Purify with a 0 to 100% ethyl acetate in hexanes gradient on silica gel to afford 0.102 g (64%) of the titled product. Rf=0.51 (1/1 hexanes/ethyl acetate). MS (m/z): 446

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968585B2
Source datasetuspto-grants-2011_06
ORD IDord-2597bae66b754075b52edefabcd8e11f
Source noteuspto-grants-2011_06