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HRID 408619作成日:2026年10月26日

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

https://huagongshe.com/reaction/408619

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 7055777985%

反応条件

温度0 °C

反応手順

To a solution of 2-benzylamino-propionic acid ethyl ester (24.72 g, 1 eq.) in 114 mL of dry DCM under nitrogen was added MgSO4 (10.80 g, 0.75 eq.). The reaction was cooled to 0° C. then acetic acid (6.82 mL, 1 eq) and the above solution of chloroacetaldehyde in dry DCM (solution I) were added. Sodium triacetoxyborohydride (38 g, 1.5 eq.) was added portionwise. The reaction was stirred for 2 h at 0° C. The crude was carefully quenched with 160 mL of a saturated aqueous solution of NaHCO3. Then 75 mL of an aqueous solution of NaOH (2N) was added. The aqueous layer was extracted twice with 120 mL of DCM. The combined organic layers were washed twice with 120 mL of a saturated aqueous solution of NaHCO3, then dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc: 100/0 to 93/7) to afford 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester (27.40 g, yield=85%).

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-830532152db6491fb68b6c30fd1135a0
出典メモuspto-grants-2014_06