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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254728Generated: October 31, 2026

Sodium Iodide → Benzeneacetic acid, 3,4-dihydroxy-5-nitro-alpha-oxo-, ethyl ester

https://huagongshe.com/reaction/2254728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
ReactantSilicon tetrachlorideHCID 24816—
ReactantEthyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylateHCID 14450984—
SolventTolueneHCID 1140—
ProductBenzeneacetic acid, 3,4-dihydroxy-5-nitro-alpha-oxo-, ethyl esterHCID 5747976—

Reaction Steps

A suspension of 17.2 g of ethyl 4-hydroxy-3-methoxy-5-nitrophenylglyoxylate in 100 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236952
Source datasetuspto-grants-1993_08
ORD IDord-5dce6a7decac409992f0d627b093b512
Source noteuspto-grants-1993_08