HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737148Generated: October 26, 2026
Ethyl cyclohexylideneacetate → 2-Cyclohexylideneethanol
https://huagongshe.com/reaction/1737148
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl cyclohexylideneacetate | HCID 73776 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Cyclohexylideneethanol | HCID 70271 | — |
Reaction Steps
To a stirred solution of ethyl cyclohexylideneacetate (see route to this by Wadsworth and Emmons in Org. Synth. Coll. Vol 5 547) (3.00 g, 17.8 mmol) in dry ether (50 ml) under an atmosphere of nitrogen at 0° C. was added lithium aluminium hydride (407 mg, 10.7 mol) portionwise and the mixture stirred for 2 hours before quenching with dilute hydrochloric acid (2M; 20 ml). The mixture was filtered and the aqueous layer was separated and extracted further with ether (2×25 ml) and the combined ether layers washed with water (2×25 ml) and saturated sodium chloride solution (25 ml) and then dried over MgSO4. Filtration and evaporation of the solvent and distillation of the residue gave 2-cyclohexylidene ethanol (2.16 g, bp. 112° C. at 10 mmHg [Kugelrohr]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962002 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-1b0575002b764ff9953526fade4c7f28 |
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| Source note | uspto-grants-1999_10 |
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