HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5304Generated: October 25, 2026
Diethyl Ether → HCID 178418606, compound
https://huagongshe.com/reaction/5304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 178418638 | HCID 178418638 | — |
| Reactant | HCID 178418655 | HCID 178418655 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418606 | HCID 178418606 | — |
Reaction Steps
A solution of nonylmagnesium bromide (8.3 mmol) in 30 ml of diethyl ether was treated at 0° C. with a solution of 1.5 g of trans-4-(4'-cyano-4-biphenylyl)cyclohexyl tetrahydropyranyl ether in 15 ml of tetrahydrofuran. The reaction mixture was heated at slight reflux overnight and then treated with dilute sodium carbonate solution. The organic phase was separated and the aqueous phase was back-extracted three times with 50 ml of diethyl ether each time. The combined organic phases were washed once with dilute sodium carbonate solution and twice with water and then dried over magnesium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9:1). The trans-4-(4-decanoyl-4-biphenylyl)cyclohexyl tetrahydropyranyl ether (1.8 g) obtained was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244597 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-5ec990aeb1174b278ed38ed7122071bb |
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| Source note | uspto-grants-1993_09 |
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