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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779375Generated: October 30, 2026

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

https://huagongshe.com/reaction/1779375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazaldHCID 6628—
ReactantDiazomethaneHCID 9550—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Cyano-6-phenyl-1-hexen-1-olHCID 67721648—
SolventEthanolHCID 702—
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 Diazald® 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 numberUS05627189
Source datasetuspto-grants-1997_05
ORD IDord-76dbd0cc59574a2693beb94c3f6559bc
Source noteuspto-grants-1997_05