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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1473075생성일: 2026년 10월 25일

Trimethylsilyldiazomethane → Methyl 2-iodo-6-methylbenzoate

https://huagongshe.com/reaction/1473075

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참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물2-Iodo-6-methylbenzoic acidHCID 9856531—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Methyl 2-iodo-6-methylbenzoateHCID 2365527776%

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온도0 °C

반응 단계

A solution of 2-iodo-6-methylbenzoic acid (I57) (2.50 g, 9.54 mmol) in DCM (30 mL) and methanol (8 mL) under an atmosphere of nitrogen was cooled to 0° C. and trimethylsilyldiazomethane (2.0 M in diethyl ether, 9.54 mL, 19.1 mmol) was added dropwise. The reaction was stirred at 0° C. for 45 minutes and then quenched with 2 M aq. HCl (50 mL). DCM (150 mL) was added to the quenched reaction and the layers were separated. The aqueous layer was extracted with DCM (100 mL), the organics were combined and washed with sat. aq. NaHCO3 (100 mL), water (100 mL), brine (100 mL), dried (MgSO4), filtered and concentrated in vacuo to give a yellow oil. The crude product was purified by silica gel chromatography (Biotage Isolera, 40 g Si Cartridge, 0-20% EtOAc in petroleum benzine 40-60° C.) to give the title compound (I58) (2.00 g, 76% yield) as a colourless oil; 1H NMR (400 MHz, CDCl3) δ 7.65 (ddd, J=7.9, 1.0, 0.5 Hz, 1H), 7.19-7.15 (m, 1H), 6.99 (t, J=7.8 Hz, 1H), 3.95 (s, 3H), 2.33 (s, 3H). LCMS Method C: rt 6.08 min; m/z 277.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012461B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-103797eb97414b7e9305193793a1a6c7
출처 메모uspto-grants-2015_04