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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855207생성일: 2026년 10월 24일

4-tert-Butylbenzaldehyde → [Rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amine

https://huagongshe.com/ko/reaction/855207

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylbenzaldehydeHCID 70324—
반응물2-Amino-1-(4-chlorophenyl)ethan-1-olHCID 412434—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
용매Water ethylacetateHCID 22728543—
생성물[Rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amineHCID 69342320—

반응 단계

1 ml of 4-tert-butylbenzaldehyde (6.15 mmol) and 960 mg of [rac]-2-amino-1-(4-chloro -phenyl)-ethanol (estimated 4.1 mmol) were dissolved in 40 ml methanol at rt, and after stirring for 5 min at rt, were refluxed for 2 h. After cooling down to rt, 310 mg (8.2 mmol) of sodium borohydride were added and after stirring for 15 min at rt, the reaction mixture was then refluxed for 2 h. After cooling down to rt, 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 stirred with a small quantity of diethylether/heptane, filtered and the solid dried under high vacuo, leading to 723 g of [rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amine as a white solid (55%). MS (ISP) 318.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-639939a6e94546d8a4bbb53f9d41552b
출처 메모uspto-grants-2007_08