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HRID 746189作成日:2026年10月27日

Pivalaldehyde → 2,2,4,4-Tetramethylpentan-3-ol

https://huagongshe.com/reaction/746189

反応式

関与物質

役割名称HCID仕込み量
反応物PivalaldehydeHCID 12417—
反応物HCID 178418306HCID 178418306—
溶媒TetrahydrofuranHCID 8028—
生成物2,2,4,4-Tetramethylpentan-3-olHCID 139790—

反応手順

To a solution of trimethylacetaldehyde (5.12 g, 59.4 mmol) in anhydrous tetrahydrofuran (15 ml) at -78° C. under an argon atmosphere is added 40.9 ml of a solution of t-butyllithium in hexanes (1.6M, 65.4 mmol). The mixture is allowed to warm from -78° to room temperature over 2 hours. The reaction is quenched with 25 ml of 1M hyrochloric acic and the resulting mixture extracted with two 25 ml portions of ether. The combined ethereal extracts were washed with saturated sodium bicarbonate solution and water, dried over magnesium sulfate, and the solvent evaporated to yield a yellow oil (9.3 g) which is purified by vacuum distillation to yield a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04603011
出典データセットuspto-grants-1986_07
ORD IDord-b51e38b89b8a4eb4ae0ac0a01d7c086a
出典メモuspto-grants-1986_07