HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862500Generated: October 26, 2026
Water → [3-Methoxy-4-(3-phenyl-prop-2-ynyloxy)-phenyl]-acetonitrile
https://huagongshe.com/reaction/1862500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-Hydroxy-3-methoxyphenylacetonitrile | HCID 78220 | — |
| Reactant | 3-Phenylprop-2-yn-1-yl 4-methylbenzene-1-sulfonate | HCID 10517333 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [3-Methoxy-4-(3-phenyl-prop-2-ynyloxy)-phenyl]-acetonitrile | HCID 18619867 | — |
Reaction Steps
A mixture of (4-hydroxy-3-methoxy-phenyl)-acetonitrile (17.4 g) and sodium cyanide (6.6 g) in dimethylformamide (250 ml) is stirred under an atmosphere of nitrogen for 3 hours at +120° C. The mixture is then cooled to +60° C. and toluene-4-sulfonic acid 3-phenyl-prop-2-ynyl ester (39 g) in dimethylformamid (50 ml)is added during 5 minutes. It is stirred at +65° C. for another 4 hours. Upon cooling water (800 ml) is added. The mixture is extracted with ethyl acetate (2×500 ml). The organic phases are washed with brine (2×500 ml), dried (MgSO4) and evaporated. The residue is purified by flash column chromatography on silica gel (ethyl acetate/hexane 1:3) and recrystallised from ethyl acetate/hexane. [3-Methoxy-4-(3-phenyl-prop-2-ynyloxy)-phenyl]-acetonitrile is obtained, m.p. 74-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06538016B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-7b7e705f691246bf9880ccde96e9e202 |
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| Source note | uspto-grants-2003_03 |
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