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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167302Generated: November 1, 2026

Nitroethane → 2-Hydroxy-4-methoxybenzonitrile

https://huagongshe.com/reaction/1167302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product2-Hydroxy-4-methoxybenzonitrileHCID 1142368086%

Reaction Steps

A mixture of the 2-hydroxy-4-methoxybenzaldehyde (20 g, 128.8 mmol), sodium acetate (35.05 g, 257.6 mmol) and nitroethane (19 mL, 257.6 mmol) in glacial acetic acid (100 mL) was heated at gentle reflux for 12 h. The reaction mixture was then poured into ˜1000 mL of ice water (1:1 ratio of ice and water). The product was extracted with ethyl acetate (3×200 mL). The organic extracts were washed with sodium bicarbonate solution until the aqueous layer had pH ˜8. The organic layers were then dried over anhydrous magnesium sulfate, and concentrated in vacuo to afford 2-hydroxy-4-methoxy-benzonitrile as a yellow oil (16.5 g, 86%). It was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617346B1
Source datasetuspto-grants-2003_09
ORD IDord-c090b9c87cff4e3caad28aa87a16a194
Source noteuspto-grants-2003_09