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HRID 1280942作成日:2026年10月27日

1-Chloro-4-(chloromethyl)benzene → (R)-tert-Butyl (1-(4-chlorobenzyl)pyrrolidin-3-yl)carbamate

https://huagongshe.com/reaction/1280942

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
反応物N,N-DipropylethylamineHCID 519799—
反応物tert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
溶媒DimethylformamideHCID 6228—
生成物(R)-tert-Butyl (1-(4-chlorobenzyl)pyrrolidin-3-yl)carbamateHCID 1842622480.2%

反応条件

温度70 °C

反応手順

4-Chlorobenzyl chloride (4.15 g, 25.8 mmol) and Pr2NEt (6.67 g, 51.6 mmol) were added to a solution of 3-{(tert-butoxycarbonyl)amino}pyrrolidine (4.81 g, 25.8 mmol) in DMF (50 mL). The reaction mixture was stirred at 70° C. for 15 h and the solvent was removed under reduced pressure. Recrystallization (CH3CN, 50 mL) provided the desired material, 3-(tert-butoxycarbonyl)amino-1-(4-chlorobenzyl)pyrrolidine as a pale yellow solid (6.43 g, 80.2%): 1H NMR (CDCl3, 300 MHz) δ1.37 (s, 9 H), 1.5-1.7 (br, 1 H), 2.1-2.4 (m, 2 H), 2.5-2.7 (m, 2 H), 2.83 (br, 1 H), 3.57 (s, 2 H), 4.1-4.3 (br, 1 H), 4.9-5.1 (br, 1 H), 7.15-7.35 (br, 4 H); The purity was determined by RPLC/MS (98%); ESI/MS m/e 311.0 (M++H, C16H24ClN2O2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06451842B1
出典データセットuspto-grants-2002_09
ORD IDord-54f1d3fce4e2444bb60cb84022f1d644
出典メモuspto-grants-2002_09