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HRID 1352199생성일: 2026년 10월 26일

1-oxo-2,3-dihydro-1H-indene-5-carbonitrile → 1-hydroxy-2,3-dihydro-1H-indene-5-carbonitrile

https://huagongshe.com/reaction/1352199

반응식

참여 물질

역할이름HCID투입량
반응물1-oxo-2,3-dihydro-1H-indene-5-carbonitrileHCID 312896—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물1-hydroxy-2,3-dihydro-1H-indene-5-carbonitrileHCID 1451532371.2%

반응 단계

A solution of 5-cyano-1-indanone (3.40 g, 21.63 mmol, prepared according to Reich, S. H., et. al. J. Med. Chem., 2000, 43, 1670–1683) in methanol (50 mL) was treated with sodium borohydride (0.25 g, 6.48 mmol). After stirring for 3 h, the reaction was diluted with methylene chloride (50 mL) and washed with saturated aqueous sodium bicarbonate (50 mL). The aqueous layer was further extracted with methylene chloride (2 50 mL). The extracts were combined, dried over magnesium sulfate and concentrated in vacuo. Silica gel chromatography eluting with 40% ethyl acetate/hexanes gave 2.45 g (15.40 mmol, 71%) of the title compound as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.48–7.54 (m, 3H), 5.25–5.29 (m, 1H), 3.03–3.10 (m, 2H), 2.81–2.89 (m, 2H), 2.52–2.59 (m, 2H), 1.94–2.01 (m, 2H); 13C NMR (CDCl3, 125 MHz) δ 150.1, 144.2, 130.9, 128.6, 125.0, 119.1, 111.8, 75.9, 35.8, 29.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220734B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-c1a5dd50cd2541859680b41914f1deac
출처 메모uspto-grants-2007_05