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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742437생성일: 2026년 10월 24일

1-Indanone → 1-Phenyl-1H-indene

https://huagongshe.com/ko/reaction/742437

반응식

참여 물질

역할이름HCID투입량
반응물1-IndanoneHCID 6735—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178506676HCID 178506676—
용매Diethyl EtherHCID 3283—
생성물1-Phenyl-1H-indeneHCID 51967445.82%

반응 단계

To a solution of 1-indanone (23.78 g, 0.18 mol) in 250 mL of ether at 0° C. was added dropwise over 30 min, 100 mL of phenyllithium in ether (1.8M in ether) and the mixture was allowed to warm to room temperature and stirred for 1 h. The reaction mixture was poured into a cold saturated ammonium chloride solution, extracted with ether (2×200 mL), and the combined organic layer was washed with brine and dried over sodium sulfate. The organic solvent was removed under reduced pressure, 70 mL of 20% sulfuric acid in acetic acid was added to the residue and stirred 2 min. To the above solution water (100 mL) and ether (3×200 mL) were added, The organic layer was washed with sodium bicarbonate solution, dried over sodium sulfate, filtered, and concentrated. Toluene (300 mL) was added to the residue and the mixture was distilled (azeotropic removal of acetic acid) to afford a brown oil. The brown oil was purified by chromatography (silica; (2:1 hexane/methylene chloride)) to afford 15.58 g (45.82%) of 1-phenyl-indene as a colorless oil. In addition 11 g of 1-phenyl-1-acetoxy-indane was isolated as a by-product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05554620
출처 데이터셋uspto-grants-1996_09
ORD IDord-890be990912541a2870722549e83916a
출처 메모uspto-grants-1996_09