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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant2-(3-Methoxy-benzyl)-cyclohexanoneHCID 14868016—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Solventtert butanol DMEHCID 86596206—
Product1-Cyano-2-[(3-methoxyphenyl)methyl]cyclohexaneHCID 1935849286.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025375
Source datasetuspto-grants-2000_02
ORD IDord-8fc6da633c114998b50b57fe3fdebd3a
Source noteuspto-grants-2000_02