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HRID 1677384作成日:2026年10月27日

Methyl iodide → 4-Methylthiane-4-carbonitrile

https://huagongshe.com/reaction/1677384

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Thiane-4-carbonitrileHCID 21598641—
溶媒TetrahydrofuranHCID 8028—
生成物4-Methylthiane-4-carbonitrileHCID 6734497853.4%

反応手順

A solution of tetrahydro-thiopyran-4-carbonitrile (3.05 g, 24 mmol) in anhydrous tetrahydrofuran (60 ml) was cooled to −78° C. and treated with lithium bis(trimethylsilyl)amide (1M in tetrahydrofuran, 26.4 ml, 26.4 mmol) dropwise. After 30 minutes of stirring, iodomethane (1.8 ml, 29 mmol) was added dropwise. The cooling bath was removed, and the reaction mixture was allowed to slowly rise to room temperature and stir overnight. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The organic layers were collected, dried over MgSO4, filtered, and concentrated giving an orange oil. The oil was purified by silica gel chromatography using 5-50% EtOAc in hexanes as eluant to provide 1.81 g (53%) of 4-methyl-tetrahydro-thiopyran-4-carbonitrile as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008298B2
出典データセットuspto-grants-2011_08
ORD IDord-90cd095f84b949b9bafdd17d6a3c678a
出典メモuspto-grants-2011_08