돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10178생성일: 2026년 10월 24일

Trifluoroacetic acid → 1-Benzyl-3-(naphthalen-2-ylmethyl)piperazine

https://huagongshe.com/ko/reaction/10178

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Ammonium HydroxideHCID 14923—
반응물4-Benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl esterHCID 21041081—
용매DichloromethaneHCID 6344—
생성물1-Benzyl-3-(naphthalen-2-ylmethyl)piperazineHCID 21978815—

반응 단계

To a solution of 4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester (0.75 g) in dichloromethane (3 mL) was added dropwise trifluoroacetic acid (3 mL). After 75 min at room temperature the mixture was poured onto ice and made basic by the addition of ammonium hydroxide (25% solution). The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were dried over magnesium sulphate, filtered, and concentrated in vacuo to afford 1-benzyl-3-(naphthalen-2-ylmethyl)piperazine as an oil; 053 g (93%) MH+ 317, Rf 0.61 (CH2Cl2/MeOH/NH4OH 93/7/0.5), which was used as such.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094779B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-dbc56614992c4ee4a364e93a778a758a
출처 메모uspto-grants-2006_08