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HRID 520352作成日:2026年10月25日

Di-tert-butyl dicarbonate → HCID 10331393、化合物

https://huagongshe.com/reaction/520352

反応式

関与物質

役割名称HCID仕込み量
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物(S)-3-Azido-4,4-dimethyldihydrofuran-2(3H)-oneHCID 10057735—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 10331393HCID 10331393—

反応手順

To a solution of (S)-3-azido-4,4-dimethyldihydrofuran-2(3H)-one (5.52 g) in MeOH 910 mL) was added 10% Pd/C (0.379 g, 0.356 mmol) under N2. The reaction mixture was stirred under H2 at rt for 16 hrs. The reaction was filtered through diatomaceous earth (Celite®), washed with EtOAc and the filtrate was concentrated to yield a clear oil. To the above oil in DCM (10 mL) was added BOC2O (9.09 mL) and TEA (13.88 mL). The reaction mixture was stirred at rt for 16 hrs. The reaction mixture was diluted with EtOAc, washed with sat. NaHCO3, citric acid, water, sat. NaCl, dried over anhydrous Na2SO4, filtered and concentrated to yield an oil. The crude product was purified by silica gel chromatography (0-100% EtOAc in hexane) to yield (S)-tert-butyl 4,4-dimethyl-2-oxotetrahydrofuran-3-ylcarbamate (3.8 g) as a white solid. LC/MS (Cond. N-1): [M+Na]+ 252.06, RT=2.75 min. 1H NMR (400 MHz, CHLOROFORM-d) ppm 4.81-4.95 (1H, m), 4.38 (1H, d, J=7.78 Hz), 3.97-4.07 (2H, m), 1.47 (9H, s), 1.25 (3H, s), 1.01 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326973B2
出典データセットuspto-grants-2016_05
ORD IDord-2500128def064324a78f9ab3b52dfdd6
出典メモuspto-grants-2016_05