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3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)- → 4-(R)-[3-(3-Acetoxyphenyl)-1-(R)-hydroxy-2-(S)-nitropropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)- | HCID 178792 | — |
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | Acetic acid 3-(2-nitroethyl)-phenyl ester | HCID 68563888 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(R)-[3-(3-Acetoxyphenyl)-1-(R)-hydroxy-2-(S)-nitropropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester | HCID 68560986 | 43% |
反応手順
Dissolve acetic acid 3-(2-nitroethyl)-phenyl ester (25.53 g, 121.6 mmol) and tert-butyl (R)-(+)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate (Gardner's aldehyde) (22.38 g, 97.61 mmol) in dry tetrahydrofuran (200 mL). Cool in ice bath and add tetrabutylammonium fluoride (98 mL, 98 mmol, 1.0 M in tetrahydrofuran) and stir for 15 minutes. Pour into ice water (2.7 L), wash with 1 N hydrochloric acid (200 mL), saturated aqueous sodium chloride, dry (magnesium sulfate), filter through a pad of silica gel and concentrate. Purify using silica gel chromatography, eluting with 5:95 ethyl acetate:dichloromethane, followed by 2 separate crystallizations using hexanes/dichloromethane to give the desired compound (18.372 g, 43% total yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07745438B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-2f7897f64e5247c789115d364de75882 |
| 出典メモ | uspto-grants-2010_06 |