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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227108Generated: October 26, 2026

Water → HCID 178444439, compound

https://huagongshe.com/reaction/2227108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-PentylcyclohexanalHCID 14085659—
Reactant[3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromideHCID 18471791—
ReactantButyllithiumHCID 178418339—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178444439HCID 178444439—

Reaction Steps

To a solution of [3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide 3D (R=pentyl) (1.68 g) in tert-butyl methyl ether at room temperature is added, dropwise, a 2.6 M solution of butyllithium (1.25 mL). The orange reaction mixture is stirred for 30 minutes, then a solution of cyclohexanal 3F (R=pentyl) (0.558 g) in tert-butyl methyl ether (3 mL) is added dropwise. The reaction is stirred a further 30 minutes, then poured into water and extracted with ether. The combined organic layers are washed with brine, then dried over sodium sulfate. The solvent is removed in vacuo and the residual material is flash chromatographed using 10% ethyl acetate in hexanes as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413448B1
Source datasetuspto-grants-2002_07
ORD IDord-d061030504034931b997d04d806f93a4
Source noteuspto-grants-2002_07