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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855200생성일: 2026년 10월 24일

Hydrochloric Acid → (4-Tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amine

https://huagongshe.com/ko/reaction/855200

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물4-tert-ButylbenzaldehydeHCID 70324—
반응물Sodium borohydrideHCID 4311764—
반응물2-(4-(Difluoromethoxy)phenyl)ethan-1-amine hydrochlorideHCID 53444441—
용매MethanolHCID 887—
생성물(4-Tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amineHCID 6934197880%

반응 단계

1.12 ml of 4-tert-butylbenzaldehyde (6.71 mmol), 1 g of 2-(4-difluoromethoxy-phenyl)-ethylamine hydrochloride (4.47 mmol) and 618 mg of potassium carbonate (4.47 mmol) were suspended in 13 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2 h. After cooling down to rt, 254 mg (6.71 mmol) sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was then refluxed for 2.5 h. After cooling down to rt, the reaction mixture was treated with 1.2 ml 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 1:4) to give 1.19 g light yellow oil (80%). MS (ISP) 334.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-83457a1aaa0b45129d2de660cfba4e43
출처 메모uspto-grants-2007_08