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HRID 1751355作成日:2026年10月25日

Water → 2-Tert-butoxycarbonylamino-3-difluoromethoxy-butyric acid methyl ester

https://huagongshe.com/reaction/1751355

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
反応物Methyl 2-{[(tert-butoxy)carbonyl]amino}-3-hydroxybutanoateHCID 4351132—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物2-Tert-butoxycarbonylamino-3-difluoromethoxy-butyric acid methyl esterHCID 7233794136.1%

反応条件

温度45 °C

反応手順

To a mixture of 2-tert-butoxycarbonylamino-3-hydroxy-butyric acid methyl ester (630 mg, 2.70 mmol) and copper(I) iodide (105 mg, 0.55 mmol) in acetonitrile at 45° C. was added a solution of 2-(fluorosulfonyl)difluoroacetic acid (0.560 mL, 5.42 mmol) in acetonitrile (2 mL) by syringe pump over 45 minutes. The reaction was then stirred at 45° C. for 30 minutes. Another solution of 2-(fluorosulfonyl)difluoroacetic acid (0.560 mL, 5.42 mmol) in acetonitrile (2 mL) was added by syringe pump over 45 minutes at 45° C. The reaction was stirred for 30 minutes at 45° C. after the second syringe pump addition was complete. Water was carefully added to quench the reaction, and the mixture was diluted with ethyl acetate. The organic layer was separated, washed with water and brine, dried (MgSO4) and concentrated. The crude material was purified by flash chromatography (10% ethyl acetate/hexanes) to yield 2-tert-butoxycarbonylamino-3-difluoromethoxy-butyric acid methyl ester (276 mg, 36%). 1H-NMR: 400 MHz, (CDCl3: 6.16 (t, JHF=74.0 Hz, 1H), 5.23-5.16 (br, 1H), 4.86-4.80 (m, 1H), 4.40 (br d, J=9.8 Hz, 1H), 3.76 (s, 3H), 1.46 (br s, 9H), 1.36 (d, J=6.4 Hz, 3H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09156823B2
出典データセットuspto-grants-2015_10
ORD IDord-b2c0e32731fb4d05be3d5e24570ddc2b
出典メモuspto-grants-2015_10