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HRID 2186548作成日:2026年10月26日

Dimethylformamide → 3-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-aldehyde

https://huagongshe.com/reaction/2186548

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物HexaneHCID 8058—
反応物3-Bromo-2-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthaleneHCID 11078647—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-aldehydeHCID 23002511—

反応条件

温度-78 °C

反応手順

A solution of 5.43 g of 3-bromo-2-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene in 110 ml of THF was cooled to −78° C. with an acetone/dry ice bath and treated dropwise with 14.5 ml of butyllithium 1.6M in hexane (1.5 eq.). The mixture was kept at −78° C. for 1 hour. DMF (2.4 ml) was added at −78° C. The reaction mixture was stirred at −78° C. for 15 min. then was allowed to warm to room temperature for 2 hours. The mixture was quenched with water (100 ml) and the pH was adjusted to 2 with hydrochloric acid 25%. The mixture was extracted with 3 portions of 100 ml of ether. The combined organic extracts were washed with water (100 ml) and saturated aqueous sodium chloride solution (100 ml). The organic phase was dried over MgSO4, filtered and concentrated in vacuo, giving a yellow oil. The product was purified by flash chromatography (SiO2, hexane then 5% ethyl acetate/hexane) yielding 4.41 g of a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06403810B2
出典データセットuspto-grants-2002_06
ORD IDord-05406ed780014e1f912c4c4f2b1a3fe7
出典メモuspto-grants-2002_06