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HRID 239772作成日:2026年10月23日

Propane sultone → 3-{[(1S)-2-tert-butoxy-1-methyl-2-oxoethyl]amino}-1-propanesulfonic acid

https://huagongshe.com/ja/reaction/239772

反応式

関与物質

役割名称HCID仕込み量
反応物Propane sultoneHCID 14264—
反応物L-Alanine 1,1-dimethylethyl esterHCID 89016—
溶媒TetrahydrofuranHCID 8028—
生成物3-{[(1S)-2-tert-butoxy-1-methyl-2-oxoethyl]amino}-1-propanesulfonic acidHCID 1603606154%

反応手順

To a solution of L-Alanine tert-butylester (1.53 g, 10.5 mmol) in tetrahydrofuran (20 mL) was added 1,3-propanesultone (1.16 g, 9.6 mmol). The solution stirred at reflux for 2 hours. The reaction was cooled to room temperature. The solid was collected by filtration and washed with acetone (2×20 mL). The solid was dissolved in water (80 mL). Dowex Marathon C ion exchange resin (strongly acidic) was added to the solution. The suspension was stirred for 15 minutes before the resin was removed by filtration. The filtrate was evaporated under reduced pressure. The solid was suspended in acetone (80 mL), filtered and dried in the vacuum oven (50° C.), affording the title compound (1.37 g, 54%). 1H NMR (D2O, 500 MHz) δ ppm 3.88 (m, 1H), 3.09 (m, 2H), 2.86 (t, 2H, J=7.3 Hz), 2.00 (m, 2H), 1.39 (d, 3H, J=7.3 Hz), 1.35 (s, 9H). 13C (D2O, 125 MHz) δ ppm 169.13, 86.12, 56.24, 47.94, 44.71, 27.11, 21.52, 14.17. [α]D=−1.1° (c=0.0027 in water), ES-MS 266 (M−1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642801B2
出典データセットuspto-grants-2014_02
ORD IDord-4546b68b7e9e4606a04b55abd139f7a0
出典メモuspto-grants-2014_02