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HRID 1375264作成日:2026年10月26日

Carbon Dioxide → 1(5-Methyl-thien-2-yl)3,4-dihydro-4,4-diethyl-7-naphthaldehyde

https://huagongshe.com/reaction/1375264

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物DimethylformamideHCID 6228—
反応物PentaneHCID 8003—
反応物TetrahydrofuranHCID 8028—
反応物1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthaleneHCID 18620062—
反応物HCID 178418306HCID 178418306—
溶媒Diethyl EtherHCID 3283—
生成物1(5-Methyl-thien-2-yl)3,4-dihydro-4,4-diethyl-7-naphthaldehydeHCID 21079515—

反応手順

To a cold (−78° C.) solution of 1-(5-methyl-thien-2-yl)-3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene (Compound F, 1.35 g, 4.1 mmol), in THF (20 mL) was added t-BuLi in pentane (1.7M solution, 3.5 mL, 5.95 mmol). The reaction was stirred for 15 minutes. and DMF (600 mg, 5.8 mmol) was added and dry-ice cooling was replaced with ice-water bath. The mixture was stirred at ambient temperature for 4 hours. The reaction mixture was diluted with ether (70 mL) and washed with water (5 mL), brine (5 mL) and dried with MgSO4. Solvent was removed by distillation. The product was purified by silicagel chromatography to afford the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07166726B2
出典データセットuspto-grants-2007_01
ORD IDord-0dfef76ef84349f897b21b46838ad55b
出典メモuspto-grants-2007_01