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HRID 1038831作成日:2026年10月27日

L-Methionine → Benzyl 4-cyano-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1038831

反応式

関与物質

役割名称HCID仕込み量
反応物L-MethionineHCID 6137—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Benzyl 4-cyanopiperidine-1-carboxylateHCID 22028286—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 4-cyano-4-methylpiperidine-1-carboxylateHCID 6698070680.3%

反応条件

温度0 °C

反応手順

LiHMDS (47.6 mL, 47.6 mmol) was added dropwise via syringe to the mixture of benzyl 4-cyanopiperidine-1-carboxylate (8.00 g, 31.8 mmol, [Oakwood]) in THF (50 mL) at about −78° C. and stirred for about 1 h. Met (6.76 g, 47.6 mmol) was added dropwise via syringe at about −78° C. and the mixture was stirred overnight at rt. The solution was cooled to 0° C. and saturated aqueous NH4Cl (200 mL) was added. The mixture was extracted with DCM (3×300 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The sample was deposited onto silica gel and purified by column chromatography eluting with 10:1 pet ether/EtOAc to give benzyl 4-cyano-4-methylpiperidine-1-carboxylate (6.6 g, 74%): LC/MS (Table 2, Method i) Rt=2.03 min; MS m/z: 259 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08551981B2
出典データセットuspto-grants-2013_10
ORD IDord-636345933a4e4599a0d0118cb39ab536
出典メモuspto-grants-2013_10