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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079490Generated: October 30, 2026

Triethylamine → HCID 11433754, compound

https://huagongshe.com/reaction/2079490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbon tetrabromideHCID 11205—
ReactantDibenzylphosphiteHCID 21904359—
Reactant5-((2,4,6-Trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenolHCID 72777273—
SolventAcetonitrileHCID 6342—
ProductHCID 11433754HCID 11433754—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenol (1.9 g, 4.8 mmol) in acetonitrile (24 mL) at room temperature, was added carbon tetrabromide (1.94 g, 1.22 eq) and triethylamine (0.728 g, 1.5 eq). The resulting mixture was stirred for 10 minutes and than cooled to 0° C. in an ice-water bath. Dibenzyl phosphite (1.51 g, 1.2 eq) dissolved in acetonitrile (16 mL) was added dropwise to the cooled reaction mixture. The reaction mixture was stirred for 2 h and monitored by TLC. The reaction was terminated by dropwise addition of aqueous potassium dihydrogen phosphate (10 mL, 0.5 M). The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic extract was dried (Na2SO4) and concentrated in vacuo to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932242B2
Source datasetuspto-grants-2011_04
ORD IDord-4b95d9a43a9c4e1da96ef3cd4ff440be
Source noteuspto-grants-2011_04