Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Dibenzylphosphite | HCID 21904359 | — |
| Reactant | 5-((2,4,6-Trimethoxystyrylsulfonyl)methyl)-2-methoxy-phenol | HCID 72777273 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11433754 | HCID 11433754 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932242B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-4b95d9a43a9c4e1da96ef3cd4ff440be |
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| Source note | uspto-grants-2011_04 |
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