HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469287Generated: October 26, 2026
Hydrochloric Acid → (5-Methoxy-2-nitrophenyl)acetonitrile
https://huagongshe.com/reaction/469287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitroanisole | HCID 7485 | — |
| Reactant | 2-(4-Chlorophenoxy)acetonitrile | HCID 306444 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (5-Methoxy-2-nitrophenyl)acetonitrile | HCID 10867168 | 39.3% |
Reaction Steps
24.0 g (214 mmol) potassium-tert-butoxide in 100 mL DMF were slowly added dropwise to a solution of 13.17 g (86.0 mmol) 4-nitroanisole and 18.0 g (107 mmol) 4-chlorophenoxyacetonitrile in 50 mL DMF. The reaction mixture was stirred for 30 min at −10° C. and then poured into 300 g of a 1:1 mixture of conc. HCl and ice. After extraction with EtOAc the organic phase was washed with water, dried and concentrated to dryness by rotary evaporation in vacuo with gentle heating. The residue was treated with a 1:1 mixture of PE/EtOAc and the product that crystallised out was suction filtered. After washing with a 1:1 mixture of PE/EtOAc the crystals were dried in the air. 6.5 g of the desired product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629137B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-a5d428de0d334c369a4650bf0acf66ea |
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| Source note | uspto-grants-2014_01 |
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