HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Nitro-6-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]-1,2-benzenediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 3-Nitro-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1-(t-butyldimethylsilyloxy)-2-hydroxybenzene | HCID 60130687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 3-Nitro-6-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]-1,2-benzenediol | HCID 60130679 | — |
Reaction Steps
Tetrabutylammonium fluoride (0.77 mL, 0.769 mmol, 1M in THF) was added to a solution of 46 (0.355 g, 0.769 mmol) and glacial acetic acid (0.04 mL, 0.769 mmol) in THF (4 mL) at rt. The reaction mixture was stirred at rt for 3 h then diluted with t-BuOMe and washed successively with water and brine. The organic layer was dried (Na2SO4) and evaporated to dryness to give a crude product which was purified by column chromatography (three times—first with: EtOAc:cyclohexane 3:7+1% acetic acid, then with neat CH2Cl2 and finally with CH2Cl2:methanol 40:1) to yield ZSB-83 (65 mg, 25%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198302B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-2a0ab7575abe4c2cb1d9fe41ebcba252 |
| Source note | uspto-grants-2012_06 |