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HRID 2264665생성일: 2026년 10월 25일

Ammonium Chloride → 2-[[2-(3-Benzyloxy-phenyl)-ethyl]-(tetrahydrofuran-3-ylmethyl)amino]-N,N-dimethyl-acetamide hydrochloride

https://huagongshe.com/reaction/2264665

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물3-Furancarboxaldehyde, tetrahydro-HCID 157568—
반응물Sodium borohydrideHCID 4311764—
반응물2-[2-(3-benzyloxy-phenyl)-ethylamino]-N,N-dimethyl-acetamideHCID 59596856—
용매1,2-DichloroethaneHCID 11—
생성물2-[[2-(3-Benzyloxy-phenyl)-ethyl]-(tetrahydrofuran-3-ylmethyl)amino]-N,N-dimethyl-acetamide hydrochlorideHCID 6659120680%

반응 단계

1.06 g (22 mmol) of NaBH4 were added portionwise to a mixture 2.9 g (9.3 mmol) of 2-[2-(3-benzyloxy-phenyl)-ethylamino]-N,N-dimethyl-acetamide, 1.28 ml (14.1 mmol) of tetrahydrofuran-3-carbaldehyde and 4 g of 4 Å molecular sieves in 130 ml of 1,2-dichloroethane. The reaction mixture was stirred at room temperature overnight. Aqueous ammonium chloride was added, the solvent was removed under vacuum, the residue was extracted with ethyl acetate and the organic phase was washed with an aqueous saturated solution of K2CO3. The solvent was removed under reduced pressure and the product was dissolved in anhydrous an hydrous hydrochloric acid in ethyl acetate. The solvent was removed and the product was triturated with diethyl ether. 3.2 g (80% yield) of the title compound were isolated as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855227B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-fc38a04f6f0c439a9517ec76642b4e0e
출처 메모uspto-grants-2010_12