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HRID 466645作成日:2026年10月25日

2,4,6-Trimethylpyridine → Neryl chloride

https://huagongshe.com/reaction/466645

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Lithium ChlorideHCID 433294—
反応物NerolHCID 643820—
溶媒DimethylformamideHCID 6228—
生成物Neryl chlorideHCID 587425985%

反応条件

温度0 °C

反応手順

To a stirred solution of 10.0 g (64.83 mmol) of (Z)-3,7-dimethyl-2,6-octadien-1-ol and 9.42 mL (71.31 mmol) of 2,4,6-collidine under argon at room temperature was added dropwise 2.74 g (64.83 mmol) of lithium chloride in 30 mL of DMF. The mixture was cooled to 0° C. and treated with 5.52 mL (71.31 mmol) of methanesulfonyl chloride dropwise over 10 minutes. The reaction was stirred at 0° C. for 4 hours (solid present), then was poured into 300 mL of ice/water. The aqueous solution was washed three times with 200 mL portions of hexane. The organic layers were combined and washed with 5% KHSO4, water, saturated NaHCO3, brine, dried (MgSO4) and evaporated to provide 9.48 g (85%) of title chloride as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157027
出典データセットuspto-grants-1992_10
ORD IDord-b1564ab221984964bfcee046024bb453
出典メモuspto-grants-1992_10