反応式
[C:1]([O-:4])(=[S:3])[CH3:2].[K+].Br[C@H:7]([CH3:11])[C:8]([OH:10])=[O:9]>C(#N)C>[C:1]([S:3][C@@H:7]([CH3:11])[C:8]([OH:10])=[O:9])(=[O:4])[CH3:2]参加物
実験手順
To a light green solution of potassium thioacetate (3.94 g, 34.5 mmol) in acetonitrile (150 ml) was added a solution of (R)-2-bromopropanoic acid (4.8 g, 31 mmol) in acetonitrile (12 ml) at room temperature under an argon atomosphere. The resulting white slurry was stirred at room temperature for 2 hours then filtered. The filtrate was concentrated in vacuo. The residue was diluted in ethyl acetate (100 ml), washed with a 10% aqueous solution of potassium bisulfate (50 ml) and brine, dried (sodium sulfate), and concentrated in vacuo. The crude product (4.61 g) was purified by flash chromatography (60 g--Merck silica gel, 1:45:54 acetic acid/ethyl acetate/hexane) to afford 3.7 g of the title product as a light yellow oil; [α]D =-114° (c=0.50, methanol).
後処理
- filtrationthen filtered
- concentrationThe filtrate was concentrated in vacuo
- additionThe residue was diluted in ethyl acetate (100 ml)
- washwashed with a 10% aqueous solution of potassium bisulfate (50 ml) and brine
- dry with materialdried (sodium sulfate)
- concentrationconcentrated in vacuo
- customThe crude product (4.61 g) was purified by flash chromatography (60 g--Merck silica gel, 1:45:54 acetic acid/ethyl acetate/hexane)
出典と根拠
- ORDレコード
- ord-c8b2279e41a64123ab0db81c78305ef5
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756832
関連ノート
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