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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15698생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/15698

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TolueneHCID 1140—
반응물2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehydeHCID 131727115—
반응물HCID 178506676HCID 178506676—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물{2-(2,3,4,5-Tetramethylcyclopentadienyl)phenyl}phenylmethylalcoholHCID 13172711687%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732643B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-26e9f2d2099144b3b3ab23636d67b9e4
출처 메모uspto-grants-2010_06