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HRID 70882作成日:2026年10月24日

Potassium Carbonate → (S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylate

https://huagongshe.com/ja/reaction/70882

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物tert-Butyl bromoacetateHCID 79177—
反応物Proline benzyl ester hydrochlorideHCID 2733413—
溶媒DimethylformamideHCID 6228—
生成物(S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylateHCID 5960754849.4%

反応手順

To a suspension of (S)-benzyl pyrrolidine-2-carboxylate hydrochloride (700 mg, 2.90 mmol) and K2CO3 (1201 mg, 8.69 mmol) in DMF (7 ml), t-butyl bromoacetate (0.535 ml, 3.62 mmol) is added. After stirring for 71 hours, aqueous K2CO3 (1.5 g of K2CO3/40 ml of H2O) is added to the reaction mixture. The products are extracted with EtOAc. The organic layer is washed twice with water and once with brine, dried over K2CO3, filtered, and concentrated to give (S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylate (458 mg); HPLC retention time=1.38 minutes (condition D); MS (m+1)=320.2; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.44 (s, 9 H) 1.81-2.03 (m, 3 H) 2.13-2.14 (m, 1 H) 2.82-2.88 (m, 1 H) 3.13-3.17 (m, 1 H) 3.46 (A of AB, J=17.3 Hz, 1 H) 3.49 (B of AB, J=17.3 Hz, 1 H) 3.73 (dd, J=8.8 and 4.8 Hz, 1 H) 5.15 (A of AB, J=12.4 Hz, 1 H) 5.17 (B of AB, J=12.4 Hz, 1 H) 7.29-7.38 (m, 5 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822534B2
出典データセットuspto-grants-2014_09
ORD IDord-e5818882a6164ceba0db737e26bdcea1
出典メモuspto-grants-2014_09