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HRID 30525作成日:2026年10月26日

Isobutyric Acid → Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-Hexanoate

https://huagongshe.com/reaction/30525

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyric AcidHCID 6590—
反応物4-MethylmorpholineHCID 7972—
反応物Benzyl 3-{[(alpha-Chloroethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 21113521—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 66887904—

反応手順

A solution of (40) (0.53 g, 1.50 mmol) in isobutyric acid (1 mL) was added to a mixture of isobutyric acid (0.96 mL, 10.8 mmol) and N-methylmorpholine (1.14 mL, 10.4 mmol) at room temperature. The resulting reaction mixture was stirred at room temperature for 48 h. The reaction mixture was diluted with dichloromethane, washed successively with water, 10% aqueous NaHCO3 solution and brine, then dried over anhydrous Na2SO4. After filtration and removal of the solvent in vacuo, the residue was purified by flash chromatography on silica gel, eluting with 5% ethyl acetate in hexane to afford the title compound (41) as a mixture of two diastereomers (400 mg, 66%). 1H—NMR (CDCl3, 400 MHz): δ 0.85 (m, 6H), 1.14 (m, 8H), 1.44 (m, 3H), 1.62 (m, 1H), 2.13 (m, 1H), 2.32 (m, 2H), 2.51 (m, 1H), 3.06 (m, 1H), 3.24 (m, 1H) 4.95 (m, 1H), 5.10 (s, 2H), 6.76 (q, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423169B2
出典データセットuspto-grants-2008_09
ORD IDord-7215531b15434df8beee00b176cccbb1
出典メモuspto-grants-2008_09