関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetate | HCID 175 | — |
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Bromhydrol | HCID 166749 | — |
| 反応物 | Methoxy indanone | HCID 10866644 | — |
| 生成物 | 6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05229516 |
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| 出典データセット | uspto-grants-1993_07 |
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| ORD ID | ord-1245027b22874090b07ae6a4bca50ccb |
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| 出典メモ | uspto-grants-1993_07 |
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