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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16744생성일: 2026년 10월 23일

Sodium Hydroxide → 5-{4-[(Tert-butoxy)carbonyl]piperazin-1-yl}thiophene-2-carboxylic acid

https://huagongshe.com/ko/reaction/16744

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylateHCID 28065298—
촉매Silver NitrateHCID 24470—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물5-{4-[(Tert-butoxy)carbonyl]piperazin-1-yl}thiophene-2-carboxylic acidHCID 5431345371%

반응 조건

온도65 °C

반응 단계

A solution of tert-butyl 4-(5-formylthien-2-yl)piperazine-1-carboxylate (2.5 1 g, 8.50 mmol) in ethanol (85 ml) was added in one portion to a solution of silver (I) nitrate (10.0 g, 58.8 mmol) and sodium hydroxide (4.83 g, 120.6 mmol) in water (85 ml). This mixture was stirred and heated at 65° C. for 22 h. The mixture was cooled by the addition of ice and then filtered to remove silver salts. The filtrate was carefully evaporated to remove the ethanol and the resulting aqueous solution was filtered again through a glass-fibre pad to remove tarry material. The filtrate was then diluted with water to a total volume of 400 ml and then acidified to pH 5 with acetic acid. The precipitate was filtered off, washed with water and then dried in a vacuum oven at 45° C. overnight to give 5-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]thiophene-2-carboxylic acid (1.88 g, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-781faa25e190466ba8495e807b8bb176
출처 메모uspto-grants-2010_06