戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1606579作成日:2026年10月26日

CID 406 → Dimethyl 2-oxo-undecylphosphonate

https://huagongshe.com/reaction/1606579

反応式

関与物質

役割名称HCID仕込み量
反応物CID 406HCID 406—
反応物Methyl DecanoateHCID 8050—
反応物Dimethyl methylphosphonateHCID 12958—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Dimethyl 2-oxo-undecylphosphonateHCID 10612624—

反応手順

A solution of 49.6 g. (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml. dry tetrahydrofuran is cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution is added 188 ml. of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 40 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 36.3 g. (0.20 mole) methyl decanoate is added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture is allowed to warm to ambient temperature, neutralized with 25 ml. acetic acid and rotary evaporated to a white gel. The gelatinous material is taken up in 75 ml. water, the aqueous phase extracted with 100 ml. portions of chloroform (3x), the combined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, to give dimethyl 2-oxo-undecylphosphonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03953466
出典データセットuspto-grants-1976_04
ORD IDord-dd1dd85ce54b4e2e8e59589fd180eae7
出典メモuspto-grants-1976_04