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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1646609생성일: 2026년 10월 26일

Hydrogen Peroxide → (RS) 2-hydroxy-4-indanecarbonitrile

https://huagongshe.com/reaction/1646609

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Diisopropyl EtherHCID 7914—
반응물2,3-Dimethyl-2-buteneHCID 11250—
반응물Sodium HydroxideHCID 14798—
반응물2,3-Dihydro-1H-indene-4-carbonitrileHCID 15576113—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(RS) 2-hydroxy-4-indanecarbonitrileHCID 12857774—

반응 조건

온도0 °C

반응 단계

42 ml of a 1M solution of boran-tetrahydrofuran complex is cooled to 0° C., 3.7 ml of 2,3-dimethyl-2-butene in 20 ml of tetrahydrofuran is added and agitation is carried out for one hour 15 minutes at 0° C. 1.98 g of product obtained in Stage A in 20 ml of tetrahydrofuran is introduced at 0° C. over 40 minutes, with agitation for 1/4 hour at 0° C., and the temperature is allowed to rise to +14° C. over 3 hours. After cooling to 0° C., 5 ml of water is added drop by drop with agitation for 5 minutes, then 18 ml of 2N sodium hydroxide is introduced at +2° C., and the temperature is allowed to rise to +15° C. 18 ml of hydrogen peroxide at 30% is added slowly and the mixture is left under agitation for 17 hours. The reaction mixture is poured into 100 ml of water and 100 ml of isopropyl ether and decanted; the aqueous phase is extracted with isopropyl ether. The reunited organic phases are washed with water, dried and concentrated to dryness under reduced pressure. The residue is chromatographed on silica in a hexane-ethyl acetate mixture (6-4), and 0.15 g of expected product is obtained, and 1.15 g of impure product is obtained which is chromatographed again on silica in a hexane-ethyl acetate mixture (65-35) so as to obtain 0.74 g of expected product, M.p.=60° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05180741
출처 데이터셋uspto-grants-1993_01
ORD IDord-4ab0216b23454c2681ff253a1b1f5adf
출처 메모uspto-grants-1993_01