反応式
[NH2:1][CH:2]([C:6]([OH:8])=[O:7])[CH2:3][CH2:4][OH:5].[CH3:9][Si]([Cl:13])(C)C>CO>[ClH:13].[CH3:9][O:7][C:6](=[O:8])[CH:2]([NH2:1])[CH2:3][CH2:4][OH:5]参加物
4
実験手順
A suspension of DL-homoserine (1.00 g, 8.39 mmol) in methanol (40 mL) was placed in an ice bath. Trimethylsilyl chloride (2.34 mL, 18.5 mmol) was added dropwise via syringe. The reaction mixture gradually became homogenous and was further stirred at rt for 14 h, concentrated by rotary evaporation, and further dried under high vacuum. The crude oil thus obtained was used for the next step without further purification. 1H NMR (300 MHz, CD3OD) δ 2.00-2.24 (m, 2H), 3.70-3.80 (m, 2H), 3.85 (s, 3H), 4.12-4.22 (m, 1H). m/z (ESI) 134 [C5H11NO3+H]+.
後処理
- customwas placed in an ice bath
- concentrationconcentrated by rotary evaporation
- customfurther dried under high vacuum
- customThe crude oil thus obtained
- customwas used for the next step without further purification
出典と根拠
- ORDレコード
- ord-d611662c46944d55b138ebee7adb4308
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07399766B2
関連ノート
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