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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1357827생성일: 2026년 10월 25일

1-(2-Hydroxyethyl)piperazine → 1-[4-(2-Hydroxyethyl)piperazinyl]-3-methyl-3-(phenylmethylthio)butan-1-one

https://huagongshe.com/reaction/1357827

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Hydroxyethyl)piperazineHCID 7677—
반응물HexachloroacetoneHCID 8303—
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물3-(Benzylsulfanyl)-3-methylbutanoic acidHCID 14969982—
용매DichloromethaneHCID 6344—
생성물1-[4-(2-Hydroxyethyl)piperazinyl]-3-methyl-3-(phenylmethylthio)butan-1-oneHCID 18187907—

반응 조건

온도-78 °C

반응 단계

A mixture of 3-methyl-3-(phenylmethylthio)butanoic acid (1 g, 4.6 mmol) and hexachloroacetone were dissolved in CH2Cl2 (20 mL) and cooled to −78° C. Triphenyl phosphine was added and the mixture was stirred for 30 minutes. Hydroxyethyl piperazine (550 μL, 4.5 mmol) was added in CH2Cl2 (10 mL) dropwise. Triethylamine (630 μL, 4.5 mmol) was added in CH2Cl2 (10 mL) dropwise. The cold bath was removed and the solution was stirred for 24 hours. The solvent was evaporated. The crude mixture was poured into 1N HCl (100 mL) and washed with Et2O (2×50 mL). The aqueous layer was made basic with 10% K2CO3 in a brine solution. The product was extracted with EtOAc (3×100 mL), dried over Na2SO4, and concentrated. This gave the title compound which was used immediately in the next reaction. 1H NMR (300 MHz, CDCl3) δ 7.18-7.37 (mult, 5H), 3.8 (s, 2H), 3.6 (t, J=5 Hz, 4H), 3.4 (t, J=5 Hz, 2H), 2.45-2.65 (mult, 8H), 1.5 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06593347B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-dab5bbecfc6e43e49a8f2d75fb725af9
출처 메모uspto-grants-2003_07