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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1489315생성일: 2026년 10월 27일

Triethylamine → 2-ethyl-4-phenyl-1H-indene

https://huagongshe.com/reaction/1489315

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-Ethyl-1-hydroxy-4-phenylindanHCID 22340215—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물2-ethyl-4-phenyl-1H-indeneHCID 1783078473%

반응 단계

To a 300-ml four-necked round flask (equipped with stirrer chip, dropping funnel and thermometer) were introduced 9.78 g (41.3 mmol) of the 2-ethyl-1-hydroxy-4-phenylindan obtained above, 17.2 ml (123.8 mmol) of triethylamine, 0.25 g (2.1 mmol) of 4-dimethylaminopyridine and 98 ml of methylene chloride. In a nitrogen atmosphere under ice cooling, to the flask was dropwise added slowly a solution obtained by dissolving 6.4 ml (82.5 mmol) of methanesulfonyl chloride in 6.5 ml of methylene chloride. After the dropping was completed, the reaction was further performed for 3.5 hours. After the reaction mixture was poured into 250 ml of ice water, the organic phase was separated, and the aqueous phase was extracted twice with 50 ml of methylene chloride, followed by mixing the organic phases together. The whole organic phase was washed with a saturated NaHCO3 aqueous solution and then washed with a saturated saline solution, followed by drying with anhydrous Na2SO4. The solvent was distilled off under reduced pressure, and the residue was separated and purified by silica gel chromatography (developed with hexane) to obtain 6.56 g of the aimed product (mixture of two kinds of isomers) as a light yellow liquid (yield: 73%) The properties of the product thus obtained are described below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05677408
출처 데이터셋uspto-grants-1997_10
ORD IDord-a879a9169dde4265b8ed4a63d456505c
출처 메모uspto-grants-1997_10