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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387619생성일: 2026년 10월 25일

Sodium Hydroxide → N-[2-(2-bromophenyl)ethyl]heptan-4-amine

https://huagongshe.com/reaction/387619

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-HeptanoneHCID 31246—
반응물2-BromophenethylamineHCID 2734091—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
생성물N-[2-(2-bromophenyl)ethyl]heptan-4-amineHCID 68471618—

반응 단계

10 g of 2-bromophenethylamine and 5.71 g of 4-heptanone are dissolved in 250 cm3 of 1,2-dichloroethane at a temperature close to 20° C. 14.84 g of sodium triacetoxyborohydride and 2.9 cm3 of glacial acetic acid are added to the reaction medium. Stirring is continued for 20 h. 300 cm3 of 1M sodium hydroxide are added to the reaction medium. The aqueous phase is extracted with 3 lots of 100 cm3 of ethyl acetate. The organic phases are combined and washed with 4 lots of 100 cm3 of water then 100 cm3 of a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated using a rotary evaporator under reduced pressure (5 kPa). The yellow liquid obtained is purified by flash chromatography over silica (column: 400 g; particle size: 20-40 μm, spherical; flow rate: 30 cm3/min; eluent: 100% heptane to 70% ethyl acetate/30% heptane gradient). After concentrating the fractions under reduced pressure, 17.33 g of N-[2-(2-bromophenyl)ethyl]heptan-4-amine are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372864B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-450d2f7c2104419495a4bd4d5329b7bd
출처 메모uspto-grants-2013_02