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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19781생성일: 2026년 10월 23일

4-tert-Butylbenzaldehyde → (4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine

https://huagongshe.com/ko/reaction/19781

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylbenzaldehydeHCID 70324—
반응물3,4-DichlorophenethylamineHCID 217958—
반응물Sodium borohydrideHCID 4311764—
촉매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
생성물(4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amineHCID 68563688102.1%

반응 단계

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.227 ml 2-(3,4-dichloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at RT, and after stirring for 30 min at RT, were refluxed for 2 h. After cooling down to RT, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at RT, the reaction mixture was then refluxed for 2 h. After cooling down to RT, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 515 mg colorless viscous oil (97%). MS (ISP) 336.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745477B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a189fa60b3d0427fa29e1260ede59189
출처 메모uspto-grants-2010_06