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HRID 28786作成日:2026年10月24日

Sulfuric Acid → Dimethyl (6-methyl-2-oxoheptyl)phosphonate

https://huagongshe.com/ja/reaction/28786

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物5-Methylhexanoic acidHCID 12344—
反応物Dimethyl methylphosphonateHCID 12958—
反応物Methyl 5-methylhexanoateHCID 519894—
反応物ButyllithiumHCID 178418339—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物Dimethyl (6-methyl-2-oxoheptyl)phosphonateHCID 1522396876.2%

反応手順

To a solution of dimethyl methylphosphonate (2.17 ml, 20 mmol) in anhydrous THF (20 mL), cooled at −78° C. was added n-BuLi (1.6 M in hexane, 13.7 mL, 22 mmol). The mixture was stirred for 30 minutes at this temperature under nitrogen. Methyl 5-methylhexanoate (1.44 g, 10 mmol), prepared from 5-methylhexanoic acid (from Avocado) and methanol at the presence of the catalytic amount of the concentrated sulfuric acid (the procedure described in Intermediate 17.1), was added dropwise for 10 minutes. The mixture was stirred for 2 hours at −78° C., gradually was warm to room temperature. The mixture was quenched with addition of 1N HCl to pH 4-5. The organic layer was separated, washed with brine and dried over MgSO4. The residue was purified through flash chromatography on silica gel (EtOAc:Hexanes=1:1) to give the product (1.80 g) with colorless oil in 76% yield. 1HNMR (CD3OD, ppm) δ 0.866 (d, J=6.5 Hz, 6H), 1.16 (m, 2H), 1.56 (m, 3H), 2.58 (t, J=7.3 Hz, 2H), 3.10 (d, J=22.7 Hz, 2H), 3.70 (s, 3H), 3.79 (s, 3H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419999B2
出典データセットuspto-grants-2008_09
ORD IDord-002ca54a27b442f1985da6a42793eac5
出典メモuspto-grants-2008_09