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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1710601생성일: 2026년 10월 26일

4-(5-Nitro-2-trifluoromethoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester → 4-(5-Amino-2-trifluoromethoxy-phenyl)-piperazine-1-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/1710601

반응식

참여 물질

역할이름HCID투입량
반응물4-(5-Nitro-2-trifluoromethoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 67094789—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
용매Ethyl AcetateHCID 8857—
생성물4-(5-Amino-2-trifluoromethoxy-phenyl)-piperazine-1-carboxylic Acid tert-butyl EsterHCID 6709537397.6%

반응 단계

0.41 g of 4-(5-Nitro-2-trifluoromethoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (1.055 mmol) were dissolved in 10 mL ethyl acetate and 10 mL acetic acid. 0.12 g 10% Palladium/charcoal were added and the mixture hydrogenated for 3 h at room temperature. The catalyst was filtered over Celite, washed with ethyl acetate and the combined filtrates evaporated to dryness. The residue was treated with water, the pH adjusted to 9-10 with 1 N aquous sodium hydroxide and the aquous phase extracted twice with dichloromethane. The combined organic extracts were dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure to yield 0.372 g of the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790727B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-2bedcfa7abc741f2aa34ba263ce6204c
출처 메모uspto-grants-2010_09