HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263079Generated: October 31, 2026
Chloroacetonitrile → HCID 23350111, compound
https://huagongshe.com/reaction/263079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-(4-Chlorophenoxy)phenol | HCID 12346120 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23350111 | HCID 23350111 | 81% |
Reaction Steps
A solution of 3.78 g (0.0500 mol) of chloroacetonitrile in 10 ml of anhydrous ethanol is run over the course of 20 minutes into a solution of 1.04 g (0.0453 mol) of sodium and 10 g (0.0453 mol) of p-(p-chlorophenoxy)-phenol in 50 ml of anhydrous ethanol and the mixture is then heated to the reflux temperature for 4 hours. It is evaporated to dryness under reduced pressure and the residue is dissolved in diethyl ether, which is washed with water and with dilute sodium hydroxide solution. After drying over dry sodium sulphate and evaporating the solvent from the organic phase, 12 g of an orange-coloured oil are obtained. Purification of this oil by distillation under reduced pressure gives 9.5 g of a limpid pale yellow oil which is insoluble in water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156011 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-22e92a16118340d3b8fc875817ad0798 |
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| Source note | uspto-grants-1979_05 |
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