戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 70753作成日:2026年10月25日

Pinacolone → 5-Hydroxy-2,2,6,6-tetramethyl-3-heptanone

https://huagongshe.com/reaction/70753

反応式

関与物質

役割名称HCID仕込み量
反応物PinacoloneHCID 6416—
反応物HexaneHCID 8058—
反応物PivalaldehydeHCID 12417—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物5-Hydroxy-2,2,6,6-tetramethyl-3-heptanoneHCID 1097621095%

反応条件

温度-78 °C

反応手順

To a solution of pinacolone (10 g, 100 mmol, 1), in anhydrous THF (500 mL), at −78° C. a 2.0 M solution of lithium diisopropylamide (LDA) in hexane (60 mL, 120 mmol) over a period of 30 min. The reaction was stirred at −78° C. for another 30 min. To the resulting white suspension pivalaldehyde (10.9 mL, 100 mmol) was added drop-wise via syringe and the reaction continued for another 12 hrs at room temperature. The reaction was quenched by adding 10 mL of water. Approximately 80% THF was removed and the mixture was then poured into saturated aqueous solution of NH4Cl. The aqueous layer was extracted twice with diethyl ether (200 mL) and the organic layer was washed with plenty of water. The organic layer was then dried over MgSO4 and concentrated to give a crude yellow solid of β-hydroxy ketone (17.2 g, 95%, (2)). The crude product was recrystallized from hexane to give pure white solid with a yield of 81%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822635B2
出典データセットuspto-grants-2014_09
ORD IDord-0a949b82937b46d08d8550422d427c76
出典メモuspto-grants-2014_09