戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 408577作成日:2026年10月24日

Chloroacetaldehyde → 2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester

https://huagongshe.com/ja/reaction/408577

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroacetaldehydeHCID 33—
反応物Acetic AcidHCID 176—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Ethyl 2-(benzylamino)propanoateHCID 222273—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl esterHCID 70557779—

反応条件

温度0 °C

反応手順

To a solution of 2-benzylamino-propionic acid ethyl ester (1 eq.) in dry DCM was added MgSO4 (0.75 eq.). The reaction was cooled to 0° C. then the above solution of chloroacetaldehyde in dry DCM (solution I) and acetic acid (1 eq.) were added. Sodium triacetoxyborohydride (1.5 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C. The crude was carefully quenched with a saturated aqueous solution of NaHCO3. Then aqueous NaOH (2N) was added. The aqueous layer was extracted with DCM. The combined organic layers were washed with an aqueous saturated solution of NaHCO3, then dried over MgSO4 and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 98/2 to 95/5) to afford 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759334B2
出典データセットuspto-grants-2014_06
ORD IDord-ebec0e38facf4fb582b154836ae73339
出典メモuspto-grants-2014_06