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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 20195518 | HCID 20195518 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | alpha-Hydroxy-2-nitro-3-phenylbenzofuran-7-acetonitrile | HCID 13531663 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04143154 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-12e0b3ab466d434789a64fac5a1d5d3e |
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| Source note | uspto-grants-1979_03 |
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