HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458748Generated: October 31, 2026
4-Cyanophenol → 4-(2-Morpholin-4-ylethoxy)benzonitrile
https://huagongshe.com/reaction/1458748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| 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. is added 60% NaOH (2.2 g, 0.055 mol). The reaction mixture is 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) is added, and the reaction mixture is stirred at room temperature for about two days. There is still a small amount of starting material present so the reaction mixture is heated on a steam bath for 4 hours. The reaction mixture is cooled to room temperature and then the solvent is removed. Ice water is added to the residue, and the solid which precipitats is 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 | US05852035 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-13955a05db6d47069211996762836819 |
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| Source note | uspto-grants-1998_12 |
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