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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440948Generated: October 30, 2026

Ethanol → 1-Methoxy-2-cyano-6-phenyl-1-hexene

https://huagongshe.com/reaction/440948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiazomethaneHCID 9550—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Cyano-6-phenyl-1-hexen-1-olHCID 67721648—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Methoxy-2-cyano-6-phenyl-1-hexeneHCID 54173280—

Reaction Steps

A solution of 3.0 grams of potassium hydroxide in 6 mL of water was placed in a commercially available diazomethane generator. Ethanol, 8 mL, was added to the generator, and the contents of the generator were slowly warmed to 60° C. to 70° C. To this was added dropwise a solution of 4.6 grams (0.021 mole) of Diazaid® in a minimum amount of diethyl ether. The diazomethane generated was condensed on a cold finger and, in turn, was allowed to drip into a stirred, cooled solution of 2.5 grams (0.012 mole) of 2-cyano-6-phenyl-1-hexen-1-ol in a minimum of diethyl ether. The complete generation of diazomethane required about 30 to 45 minutes. Upon completion of the diazomethane generation, the reaction mixture was allowed to warm to ambient temperature. After this time the reaction mixture was concentrated under reduced pressure, yielding 2.4 grams of 1-methoxy-2-cyano-6-phenyl-1-hexene. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521192
Source datasetuspto-grants-1996_05
ORD IDord-283d7934c46241bdb81af1214d0d213b
Source noteuspto-grants-1996_05