HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383018Generated: October 31, 2026
Acetone → 3-Nitro-5-(1,2-dihydroxyethyl)benzoic acid methyl ester
https://huagongshe.com/reaction/383018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 3-Nitro-5-vinylbenzoic acid methyl ester | HCID 54026731 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Nitro-5-(1,2-dihydroxyethyl)benzoic acid methyl ester | HCID 54554983 | — |
Reaction Steps
3-Nitro-5-vinylbenzoic acid methyl ester (2.02 g, 9.76 mmol) was dissolved in a mixture of acetone and water (200 ml, 9:1), and, after cooling to 0° C., OsO4 (60 mg, 0.24 mmol) was added followed by N-methylmorpholine-N-oxide (2.34 g, 20.0 mmol). After stirring for 46 h at room temperature, an aqueous solution of Na2S2O5 (3.7 g) in water (150 ml) was added and the solution was acidified with dilute aqueous HCl. The volume of the solution was reduced to 150 ml by evaporation and the residue was extracted with ethyl acetate (3×100 ml). The combined organic phases were evaporated and the residue was purified by column chromatography on silica gel using ethyl acetate as the eluent. Yield: 1.60 g (60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310243B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-fc2b20c9aea348edb2c694b4c5b328c9 |
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| Source note | uspto-grants-2001_10 |
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