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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614103Generated: October 30, 2026

Diethyl Ether → alpha-Hydroxy-2-nitro-3-phenylbenzofuran-7-acetonitrile

https://huagongshe.com/reaction/614103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium CyanideHCID 8929—
ReactantHCID 20195518HCID 20195518—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Productalpha-Hydroxy-2-nitro-3-phenylbenzofuran-7-acetonitrileHCID 13531663—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred mixture of 2.7 g. (0.010 mole) of 2-nitro-3-phenylbenzofuran-7-aldehyde and 20 ml. of diethyl ether is treated with 1.6 g. (0.015 mole) of sodium bisulfite in 10 ml. of water. After 30 minutes, 30 ml. of chloroform is added and then, 30 minutes later, 1.5 g. (0.030 mole) of sodium cyanide in 5 ml. of water is added. One-half hour after that 0.7 g. of sodium bisulfite is added, then, after another 30 minutes, the mixture is cooled at 0° C. for about 16 hours. The organic layer is separated, washed with aqueous sodium bisulfite solution, then with water, and dried over magnesium sulfate. Evaporation of the solution provides a solid which is recrystallized from a chloroform-heptane mixture to provide yellow crystals of α-hydroxy-2-nitro-3-phenylbenzofuran-7-acetonitrile, m.p. 137°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143154
Source datasetuspto-grants-1979_03
ORD IDord-12e0b3ab466d434789a64fac5a1d5d3e
Source noteuspto-grants-1979_03