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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15698Generated: October 25, 2026

Water → {2-(2,3,4,5-Tetramethylcyclopentadienyl)phenyl}phenylmethylalcohol

https://huagongshe.com/reaction/15698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactant2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehydeHCID 131727115—
ReactantHCID 178506676HCID 178506676—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product{2-(2,3,4,5-Tetramethylcyclopentadienyl)phenyl}phenylmethylalcoholHCID 13172711687%

Reaction Steps

To a solution of 2-(2,3,4,5-tetramethylcyclopentadienyl)benzaldehyde (2.0 g, 8.80 mmol) in tetrahydrofuran (34.0 mL) was added dropwise a 1.05 M solution of phenyllithium in cyclohexane and ether (17.7 mL) at −78° C. The temperature of the mixture was raised to room temperature and the mixture was stirred for 4 hrs. To the reaction mixture solution were added deionized water (20.0 mL) and toluene (20.0 mL) to separate an organic layer and an aqueous layer. The organic layer was dried over sodium sulfate, then distilled to remove the solvent, and purified by a silica gel column (hexane/ethyl acetate=9/1) to give {2-(2,3,4,5-tetramethylcyclopentadienyl)phenyl}phenylmethylalcohol (2.83 g, yield 87.0%) as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732643B2
Source datasetuspto-grants-2010_06
ORD IDord-26e9f2d2099144b3b3ab23636d67b9e4
Source noteuspto-grants-2010_06