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HRID 1836862作成日:2026年10月25日

Acetic Acid → 3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthalenecarboxaldehyde

https://huagongshe.com/reaction/1836862

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物WaterHCID 962—
反応物6-Cyano-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthaleneHCID 3553439—
反応物DiisobutylaluminumhydrideHCID 21225700—
溶媒DichloromethaneHCID 6344—
生成物3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthalenecarboxaldehydeHCID 22669863%

反応手順

To a solution of 18.7 g (82.3 mmol) of 2-cyano-3-methyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene in 280 mL of dichloromethane, cooled at −78°, was added 123 mL (123 mmol) of diisobutyl aluminum hydride (1.0 M in toluene). The reaction mixture was stirred and allowed to gradually warm to room temperature. After 16 hours, the reaction mixture was treated with 30 mL of acetic acid added dropwise, followed by 150 mL of water. The organic layer was separated, diluted with 200 mL of hexane, washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (gradient elution 5-10% ethyl acetate/hexane) on silica gel to afford 11.8 g (63%) of 2-formyl-3-methyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06777418B2
出典データセットuspto-grants-2004_08
ORD IDord-c7bdc6b501db4b338bc1f72659249bd2
出典メモuspto-grants-2004_08