HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248850Generated: October 27, 2026
Acetic Acid → 2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrile
https://huagongshe.com/reaction/248850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | (-)-Menthol | HCID 16666 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrile | HCID 57204740 | — |
Reaction Steps
1 g of a sodium hydride suspension (50% strength) in paraffin oil was added at a temperature of 0° C. to a solution of 30 g of L-menthol in 300 ml of dichloromethane. A solution of 12.5 ml acrylonitrile in 50 ml dichloromethane was slowly added dropwise, and the reaction mixture was then stirred at room temperature for a further 5 hours. The reaction mixture was worked up by cautiously adding 10 ml of glacial acetic acid, followed by 200 ml of water, and then extracting the mixture with dichloromethane. The dichloromethane extract was dried over sodium sulfate, filtered and concentrated. After chromatographic purification of the residue on silica gel using n-hexane/dichloromethane as the eluent, 25.03 g of crude 2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrile were obtained and used for the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212173 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-339e1ff250f641c3b64602c0196a7803 |
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| Source note | uspto-grants-1993_05 |
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