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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324670Generated: October 30, 2026

Sodium Carbonate → HCID 86755061, compound

https://huagongshe.com/reaction/324670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTolylboronic acidHCID 79799—
ReactantHCID 86755062HCID 86755062—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 86755061HCID 8675506195%

Reaction Steps

A solution of 0.41 g (2.99 mmol) of 4-methylphenylboronic acid in 13 cm3 of methanol and 30 cm3 of a 2N aqueous sodium carbonate solution were successively added to a solution of 1.37 g (2.7 mmol) of methyl (3aRS,4SR,7aRS)-2-benzyl-7-iodo-4-(2-methoxyphenyl)-2,3,3a,4,5,7a-hexahydro-1H-isoindole-3a-carboxylate and of 0.15 g (0.13 mmol) of tetrakis(triphenylphosphine)palladium in 30 cm3 of toluene and then the mixture was brought to reflux for two hours. After returning to a temperature in the region of 20° C., the reaction mixture was extracted with 100 cm3 of ethyl acetate, washed with two times 50 cm3 of distilled water, dried over magnesium sulphate and then concentrated under reduced pressure. The brown residue obtained was purified by flash chromatography on silica gel (230-400 mesh), elution being carried out with a cyclohexane/ethyl acetate (95/05 by volume) mixture. 1.2 g (93%) of methyl (3aRS,4SR,7aRS)-2-benzyl-4-(2-methoxyphenyl)-7-(4-methylphenyl)-2,3,3a,4,5,7a-hexahydro-1H-isoindole-3a-carboxylate were thus obtained in the form of a yellow oil, the characteristics of which were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218406B1
Source datasetuspto-grants-2001_04
ORD IDord-5a4ad1afdc2d462bb780392a939e0e8f
Source noteuspto-grants-2001_04