HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725323Generated: October 27, 2026
Sodium Iodide → Benzeneacetic acid, 3,4-dihydroxy-5-nitro-alpha-oxo-, ethyl ester
https://huagongshe.com/reaction/725323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Silicon tetrachloride | HCID 24816 | — |
| Reactant | Ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate | HCID 14450984 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzeneacetic acid, 3,4-dihydroxy-5-nitro-alpha-oxo-, ethyl ester | HCID 5747976 | — |
Reaction Steps
A suspension of 17.2 g of ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate in 100 ml of dry acetonitrile and 100 ml of dry toluene is treated with 10.53 g of sodium iodide and 11.9 g of silicon tetrachloride and heated under reflux for 47 hours. The reaction mixture is then evaporated and the residue is distilled six times with 200 ml of toluene each time. The residue obtained is partitioned between water and ether and filtered through a filter aid of diatomaceous earth. The ethereal phase is washed four times with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. The oily residue is treated three times with ether and active carbon. There is obtained ethyl 3,4-dihydroxy-5-nitrophenylglyoxylate of m.p. 77°-79° (from ether/n-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05705703 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-aed7241c6d7749e2b094ed738b5a9752 |
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| Source note | uspto-grants-1998_01 |
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