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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Cyano-6-phenyl-1-hexen-1-ol | HCID 67721648 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methoxy-2-cyano-6-phenyl-1-hexene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521192 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-283d7934c46241bdb81af1214d0d213b |
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| Source note | uspto-grants-1996_05 |
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