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HRID 989262作成日:2026年10月25日

2-Methylbenzaldehyde → tert-Butyl(dimethyl){[3-(2-methylbenzylidene)-1-cyclohepten-1-yl]oxy}silane

https://huagongshe.com/reaction/989262

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylbenzaldehydeHCID 10722—
反応物TriphenylphosphineHCID 11776—
反応物2-Cyclohepten-1-oneHCID 70723—
反応物tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl(dimethyl){[3-(2-methylbenzylidene)-1-cyclohepten-1-yl]oxy}silaneHCID 69965728—

反応手順

To a solution of cycloheptenone (71.7 mmol) in 220 ml of anhydrous THF there are added, in succession, triphenylphosphine (72.6 mmol) and then, dropwise, tert-butyldimethylsilyl triflate (72.3 mmol), and the whole is stirred at room temperature for 1 hour 30 minutes. The mixture is then brought to −78° C., and a solution of nBuLi/hexane (72 mmol) is added slowly, followed 30 minutes later by 2-methylbenzaldehyde (72.03 mmol). The whole is stirred at that temperature for 30 minutes, and then with the temperature gradually returning to room temperature. After 2 hours 30 minutes, the reaction mixture is precipitated from 2.5 liters of petroleum ether and filtered, and the filtrate is concentrated to dryness. The title product is purified by chromatography over silica gel (100% heptane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638962B2
出典データセットuspto-grants-2003_10
ORD IDord-1998a41d3c444e92befe8253cdc01e54
出典メモuspto-grants-2003_10