HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613283Generated: October 29, 2026
4-Cyanophenol → 4-(2-Morpholin-4-ylethoxy)benzonitrile
https://huagongshe.com/reaction/613283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(2-Chloroethyl)morpholine | HCID 76727 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Morpholin-4-ylethoxy)benzonitrile | HCID 2994074 | 97% |
Reaction Steps
To a solution of 4-cyanophenol (5.95 g, 0.05 mol) in DMF (35 mL) at 0° C. was added 60% NaH (2.2 g, 0.055 mol). The reaction mixture was stirred at 0° C. for 15 minutes, then at room temperature for 15 minutes and then N-(2-chloroethyl)morpholine (prepared from 11.16 g, 0.06 mol of the hydrochloride salt) was added and the reaction mixture was stirred at room temperature for about 2 days. There was still a small amount of starting material present so the reaction mixture was heated on a steam bath for 4 hours. The reaction mixture was cooled to room temperature and then the solvent was removed. Ice-water was added to the residue and the solid which precipitated was collected by filtration and dried to afford 11.3 g (97%) of 4-[2-(4-morpholinyl)ethoxy]benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008226 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-69d97724e2e74d0f8404675864a1c077 |
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| Source note | uspto-grants-1999_12 |
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