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HRID 253579作成日:2026年10月26日

D-Proline → HCID 57786523、化合物

https://huagongshe.com/reaction/253579

反応式

関与物質

役割名称HCID仕込み量
反応物D-ProlineHCID 8988—
反応物1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
反応物Sodium borohydrideHCID 4311764—
反応物3-(Oxan-4-yl)propanalHCID 57449683—
溶媒EthanolHCID 702—
溶媒AcetonitrileHCID 6342—
生成物HCID 57786523HCID 5778652389%

反応条件

温度0 °C

反応手順

To a stirred solution of 3-(tetrahydro-pyran-4-yl)-propionaldehyde (8.59 g, 0.06 mol) and dibenzyl azodicarboxylate (12.8 g, 0.042 mol) in MeCN (250 mL) at 0° C. was added (R-proline) (0.48 g, 0.0042 mol). After stirring the mixture at 0° C. for 15 h, ethanol (100 mL) and NaBH4 (1.56 g, 0.042 mol) were added, and the mixture was stirred at 0° C. for 40 min. The reaction was quenched by slow addition of 10% aq citric acid (15 mL), and the whole solution was concentrated in vacuo. This residue was diluted with EtOAc (200 mL), washed with brine (50 mL), dried over Na2SO4, and concentrated in vacuo to give crude product which was purified by column chromatography to give (S)-dibenzyl 1-(1-hydroxy-3-(tetrahydro-2H-pyran-4-yl)propan-2-yl)hydrazine-1,2-dicarboxylate (16.52 g, 89%). 1H NMR (CD3OD) δ 1.0-1.5 (m, 8H), 2.9-3.3 (m, 2H), 3.4-3.6 (m, 2H), 3.7-3.9 (m, 2H), 4.4-4.7 (m, 2H), 5.1-5.4 (m, 4H), 7.2-7.4 (m, 10H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872028B2
出典データセットuspto-grants-2011_01
ORD IDord-e081292ec63447d6af8e1dcf1288bce3
出典メモuspto-grants-2011_01