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HRID 355754作成日:2026年10月25日

Acetic Acid → ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate

https://huagongshe.com/reaction/355754

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Ethyl 4-(aminomethyl)benzoateHCID 436161—
反応物2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoateHCID 22675503—

反応手順

2-Benzyloxy-5-bromobenzaldehyde and ethyl 4-aminomethylbenzoate were heated together at 100° C. for 1 hour. The mixture was cooled, dissolved in ethanol (100 ml) and sodium borohydride (1.3 g) was added. The mixture was stirred for 18 hours at ambient temperature, acidified with acetic acid and water (200 ml) was added. The mixture was extracted with diethyl ether (4×100 ml), the extracts washed with saturated aqueous NaHCO3, dried (MgSO4), filtered and evaporated to give ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate which was purified by chromatography on silica gel eluting with CH2Cl2 then 5% ethyl acetate/CH2Cl2 (yield 11.4 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834468
出典データセットuspto-grants-1998_11
ORD IDord-ac2592b1d7e9403f99739f686d9d8a9c
出典メモuspto-grants-1998_11