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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1866609생성일: 2026년 10월 27일

Trimethylsilyldiazomethane → Methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoate

https://huagongshe.com/reaction/1866609

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물2-{[2-(3,5-Difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoic acidHCID 66973305—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoateHCID 66973283—

반응 단계

To a solution of 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoic acid from Step A (400. mg, 1.46 mmol) in MeOH (3 mL), was added trimethylsilyldiazomethane (2 M in hexanes) until yellow color persists. The reaction mixture was stirred for an additional twenty minutes. The reaction mixture was diluted with ether (30 mL) and water (10 mL). The organics were washed with 5% sodium bicarbonate and then with saturated brine. The organics were dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue. This residue was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:Hexanes—40:60 to 90:10, to give the title compound. MS: m/z=229 (M−CO2Me).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07629338B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-db22292baca7472face4cdcefbeb6fec
출처 메모uspto-grants-2009_12