HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377296Generated: October 29, 2026
Diethyl Ether → 1-Cyano-2-[(3-methoxyphenyl)methyl]cyclohexane
https://huagongshe.com/reaction/377296
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 2-(3-Methoxy-benzyl)-cyclohexanone | HCID 14868016 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | tert butanol DME | HCID 86596206 | — |
| Product | 1-Cyano-2-[(3-methoxyphenyl)methyl]cyclohexane | HCID 19358492 | 86.6% |
Reaction Steps
A solution of potassium tert-butoxide (4.10 g) in tert-butanol-1,2-dimethoxyethane (1:1, 38 ml) was added dropwise to a stirred solution of 2-[(3-methoxyphenyl)-methyl]cyclohexanone (4.10 g) and (p-tolylsulfonyl)methyl isocyanide (4.10 g) in 1,2-dimethoxyethane under ice cooling over 30 minutes. The resulting mixture was stirred at the same temperature for 1 hour and at room temperature for 2 hours and 30 minutes, and then a mixture of diethyl ether and water was added thereto. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The oily residue was chromatographed over silica gel using n-hexane--ethyl acetate as an eluent to afford 1-cyano-2-[(3-methoxyphenyl)methyl]cyclohexane (3.73 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06025375 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-8fc6da633c114998b50b57fe3fdebd3a |
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| Source note | uspto-grants-2000_02 |
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