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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1670743생성일: 2026년 10월 26일

Ethylene Glycol → 1-Boc-4-(2-thienyl)piperazine

https://huagongshe.com/reaction/1670743

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물2-IodothiopheneHCID 18921—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매IsopropanolHCID 3776—
용매Ethyl AcetateHCID 8857—
생성물1-Boc-4-(2-thienyl)piperazineHCID 6734390077%

반응 단계

A mixture of 2-iodothiophene (Aldrich Co., 1.0 g), 1-(tert-butoxycarbonyl)piperazine (Aldrich Co. (hereafter the same), 1.06 g), copper(I) iodide (45 mg), ethylene glycol (530 μl), potassium phosphate (2.02 g) and 2-propanol (5 ml) was heated under reflux for 20 hr. Ethyl acetate was added, and the mixture was filtered through a Celite (trademark) filter. The filtrate was washed 3 times with 28% aqueous ammonia, and then washed with saturated brine. The solvent was evaporated under reduced pressure to give a brown solid. The solid was purified by silica gel column chromatography (elution solvent: ethyl acetate-hexane (7:3)) to give 4-(2-thienyl)piperazine-1-carboxylic acid tert-butyl ester (984 mg, yield 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07994196B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-ffc748b1030f4f6abf2f239762f169db
출처 메모uspto-grants-2011_08