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HRID 1473075作成日:2026年10月26日

Trimethylsilyldiazomethane → Methyl 2-iodo-6-methylbenzoate

https://huagongshe.com/reaction/1473075

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物2-Iodo-6-methylbenzoic acidHCID 9856531—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-iodo-6-methylbenzoateHCID 2365527776%

反応条件

温度0 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012461B2
出典データセットuspto-grants-2015_04
ORD IDord-103797eb97414b7e9305193793a1a6c7
出典メモuspto-grants-2015_04