돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21690생성일: 2026년 10월 24일

Ethyl bromoacetate → (4-Methylpiperazin-1-yl)acetic acid

https://huagongshe.com/ko/reaction/21690

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물1-MethylpiperazineHCID 53167—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물(4-Methylpiperazin-1-yl)acetic acidHCID 276273282.2%

반응 단계

Dissolve N-methylpiperazine (5.0 mL, 45.09 mmol) in diethyl ether in a stoppered flask and treat with neat ethyl bromoacetate (3.012 g, 18.036 mmol). Stir the reaction mixture at room temperature overnight, filter and wash the filter cake with diethyl ether. Combine the organic filtrates and evaporate the solvent in vacuo to give a light yellow oil. Take up in water (60 mL) and heat at 95° C. for 4 hours, allow to cool to room temperature and stir overnight. Evaporate the solvent in vacuo and dissolve the residue in acetonitrile and evaporate the solvent in vacuo (twice) to azeotrope residual water. Dissolve in a minimal amount of methanol, dilute with diethyl ether and place in the freezer. Isolate the crystals which form by decanting the supernatant and wash with diethyl ether. Obtain two more crops of crystals from the mother liquor to give 4-methylpiperazine-1-acetic acid (2.345 g, 82%); mp 158°-160° C. (lit 159.5°-161° C.), 1H NMR (D2O) δ3.98 (s, 2), 3.81-3.32 (m, 8), 2.89 (s, 3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424425
출처 데이터셋uspto-grants-1995_06
ORD IDord-8962002a73a24a579b0bd69d56bd8183
출처 메모uspto-grants-1995_06