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HRID 484241作成日:2026年10月24日

Acetate → 6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-one

https://huagongshe.com/ja/reaction/484241

反応式

関与物質

役割名称HCID仕込み量
反応物AcetateHCID 175—
反応物BenzeneHCID 241—
反応物Hydrochloric AcidHCID 313—
反応物BromhydrolHCID 166749—
反応物Methoxy indanoneHCID 10866644—
生成物6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-oneHCID 234338—

反応手順

To a stirred solution of anhydrous aluminum bromide (69.82 g, 0.261 mole) in anhydrous benzene (250 mL) kept under nitrogen is added dropwise over 30 minutes a solution of the methoxy indanone (18 g, 0.102 mole) of Step C, in benzene (60 mL). The mixture is gently refluxed for 3 hours (TLC, dichloromethaneethyl acetate 8:2, UV), cooled in an ice bath and treated dropwise with 6N-HCl (ca. 200 mL) to decompose the aluminum complex. The aqueous phase is extracted with ether (3 times), the extracts are concentrated at reduced pressure and extracted with 2.5N-NaOH (2×75 mL and 1×50 mL). The basic extracts are neutralized (ice bath) with concentrated HCl and the oil that separates is extracted with ether (3 times). The combined extracts are washed with brine, dried (MgSO4) and evaporated to yield an oil that readily solidifies. The crude material is flash chromatographed (on silica Merck-60, gradient CH2Cl2, CH2Cl2 -ethyl acetate 85:15 ) to provide the pure title compound (13.60 g, nearly colorless solid, 82%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05229516
出典データセットuspto-grants-1993_07
ORD IDord-1245027b22874090b07ae6a4bca50ccb
出典メモuspto-grants-1993_07