HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566165Generated: October 30, 2026
Methoxymethyl-triphenylphosphonium chloride → HCID 178448047, compound
https://huagongshe.com/reaction/566165
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178448051 | HCID 178448051 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178448047 | HCID 178448047 | — |
Reaction Steps
A mixture of 57.3 g (167 mmol) of methoxymethyl-triphenylphosphonium chloride and 500 ml of THF was cooled to −30° C. under a nitrogen gas stream with a refrigeration medium. 17.3 g (154 mmol) of t-BuOK was added to this mixture, followed by stirring for 1 hour. To this mixture, 300 ml of THF containing 34.0 g (129 mmol) of 3-(trans-4-(trans-4-propylcyclohexyl)cyclohexyl)propanal was added dropwise, while a temperature of −30° C. or less was maintained. After the dropping, a reaction temperature was gradually raised to room temperature, followed by stirring for 5 hours. The reaction mixture was filtered through Celite, and the solvent was then distilled off under reduced pressure. The resulting residue was purified through silica gel column chromatography (a developing solvent: heptane) to obtain 30.3 g of crude 1-methoxy-4-(trans-4-(trans-4-propylcyclohexyl)cyclohexyl)-1-butene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174459B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-9d5cb03def2f4da5a6011fc2548822fa |
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| Source note | uspto-grants-2001_01 |
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