HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464525Generated: October 25, 2026
Water → 5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile
https://huagongshe.com/reaction/1464525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-Iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutane | HCID 19088027 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile | HCID 19088086 | 163% |
Reaction Steps
To a solution of 4.19 g (5.0 mmole) of 1-iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutane in dimethylsulfoxide (30 ml) was added 0.74 g (5×3 mmole) of sodium cyanide, and the mixture was stirred at 50° C. for 2 hours. The reaction solution was cooled with ice, and isopropyl ether and water were added to it, followed by stirring. The isopropyl ether layer was separated out, washed with aqueous sodium chloride solution, dried (magnesium sulfate) and evaporated. The residual solution was chromatographed on a silica gel column to perform purification (elution with isopropyl ether/hexane) to thereby give 1.65 g (98%) of 5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile. Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05304658 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-316c513b3521443883167070cb77e4ff |
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| Source note | uspto-grants-1994_04 |
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