돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16794생성일: 2026년 10월 25일

Trimethylsilyldiazomethane → Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate

https://huagongshe.com/reaction/16794

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물4-(4-Methyl-1-piperazinylmethyl)benzoic acidHCID 4769782—
용매MethanolHCID 887—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 78222244.2%

반응 단계

A solution of (trimethylsilyl)diazomethane ((0.611 mL, 3.84 mmol) 2.0M in diethyl ether) was added dropwise to a stirred suspension of 4-((4-methylpiperazin-1-yl)methyl)benzoic acid (0.75 g, 3.20 mmol) in toluene (21 mL) and methanol (7 mL) over a period of 10 mins under nitrogen. The resulting suspension was stirred at room temperature for 3 h. A further aliquot of (trimethylsilyl)diazomethane (1.222 mL, 7.68 mmol) was added dropwise and the solution was stirred at room temperature for a further 18 h. The reaction mixture was evaporated to dryness to afford the crude product (0.723 g) as a white solid. This was taken up in DCM and the insolubles were filtered off. The filtrate was evaporated to dryness to afford the crude product. This was taken up in DCM again and more insolubles were filtered off to afford methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate (0.351 g, 44.2%), which was used without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-37f83163a3964c7e86f2f9cd86e5db68
출처 메모uspto-grants-2010_06