HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490928Generated: October 29, 2026
Diethyl Ether → 2-Hydroxy-2-(3-nitrophenyl)acetonitrile
https://huagongshe.com/reaction/490928
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxy-2-(3-nitrophenyl)acetonitrile | HCID 3277808 | 125.4% |
Reaction Steps
A mixture of a 10% solution of sodium bisulfite (24 g, 230 mmol) and 3-nitrobenzaldehyde (27 g, 178 mmol) was combined in a 1L flask with 75 mL ether and 100 ml THF. The resulting reaction mixture was cooled in an ice-water bath to 10° C. and a solution of potassium cyanide (15 g, 130 mmol) in 75 mL water was added over a period of a half-hour while stirring. The reaction mixture was stirred at 15° C. for 1 hour. The organic layers were separated and the aqueous phase was extracted with ether (200 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo to afford (3-nitrophenyl)(hydroxy)acetonitrile as a yellow oil (29 g, 163 mmol), which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528173B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-20ddc5c54e1e426983d49f5ae7b24879 |
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| Source note | uspto-grants-2009_05 |
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