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HRID 40751作成日:2026年10月23日

Trimethylsilyldiazomethane → Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate

https://huagongshe.com/ja/reaction/40751

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物1-(3-Bromo-5-cyanophenyl)piperidine-4-carboxylic acidHCID 59588189—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
生成物Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylateHCID 59588037100%

反応手順

To a solution of 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylic acid (1.1 g, 3.6 mmol) in toluene (4 mL) and methanol (2 mL) was added TMSCHN2 (2 M in Et2O, 3.5 mL, 7.0 mmol) dropwise at room temperature. After 1 h, the reaction was quenched with acetic acid (˜0.1 mL), diluted with EtOAc and washed with saturated aqueous NaHCO3. The organic layer was separated, dried (MgSO4), and concentrated to give methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate in ˜100% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530480B2
出典データセットuspto-grants-2013_09
ORD IDord-852a98529a0f4ee78c517dafdbe85afc
出典メモuspto-grants-2013_09