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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332672Generated: October 30, 2026

Sodium Carbonate → HCID 71093194, compound

https://huagongshe.com/reaction/332672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Formylphenylboronic acidHCID 2734356—
Reactant2-[(4-bromophenyl)methyl]-1,3-dioxolaneHCID 2756956—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 71093194HCID 7109319452.3%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 2-(4-bromobenzyl)-1,3-dioxolane (2.0 g, 8.2 mmol), 3-formylboronic acid (2.45 g, 16.4 mmol), tetrakis-(triphenylphosphine)palladium (0) (0.763 g, 0.66 mmol), and sodium carbonate (1.74 g, 16.4 mmol) in dioxan/water (15 mL/3 mL) in a microwave vessel was degassed in a stream of nitrogen for 10 minutes. The vessel was sealed and heated in the microwave at 125° C. for 30 minutes. The solvent was decanted off, and the solid residues washed with ethyl acetate. The organic phases were combined, and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in iso-hexane to afford an oil. The oil was dissolved in methanol (25 mL) and cooled to 0° C. Sodium borohydride (0.393 g, 10.4 mmol) was added portion-wise, and the reaction mixture was stirred at 0° C. for 30 minutes followed by 1 hour at ambient temperature. The reaction mixture was quenched with water and extracted twice with ethyl acetate. The combined organic extracts were dried with anhydrous magnesium sulfate, and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 100% ethyl acetate in iso-hexane to afford the title compound (1.16 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877774B2
Source datasetuspto-grants-2014_11
ORD IDord-0efbcbd4f500439bbcd0c6acd9dee531
Source noteuspto-grants-2014_11