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HRID 37694作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/37694

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BromhydrolHCID 166749—
反応物Methoxy indanoneHCID 10866644—
反応物Dichloromethane ethylacetateHCID 21226138—
溶媒BenzeneHCID 241—
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, dichloromethane-ethyl 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US05420289
出典データセットuspto-grants-1995_05
ORD IDord-f438f32912d145acbeea5072e94ba4fd
出典メモuspto-grants-1995_05