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HRID 392886作成日:2026年10月25日

3-Isopropyl-4-methoxybenzaldehyde → Tert-butyl 4-[hydroxy(4-methoxy-3-isopropylphenyl)methyl]-3,5-dimethylphenylcarbamate

https://huagongshe.com/reaction/392886

反応式

関与物質

役割名称HCID仕込み量
反応物3-Isopropyl-4-methoxybenzaldehydeHCID 9898990—
反応物tert-Butyl (4-bromo-3,5-dimethylphenyl)carbamateHCID 22662122—
反応物HCID 178418306HCID 178418306—
反応物HCID 178418348HCID 178418348—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒PentaneHCID 8003—
溶媒CyclohexaneHCID 8078—
溶媒Cyclohexane diethyletherHCID 21895417—
生成物Tert-butyl 4-[hydroxy(4-methoxy-3-isopropylphenyl)methyl]-3,5-dimethylphenylcarbamateHCID 2266212465.6%

反応手順

970 mg (3.23 mmol) of tert-butyl 4-bromo-3,5-dimethylphenylcarbamate (Example IV) are dissolved in 3 ml of cyclohexane and 3 ml of ether, cooled to −78° C., and added dropwise to 2.53 ml of 1.6 M methyllithium in ether at −78° C. After stirring at this temperature for 10 minutes, 3.8 ml of 1.7 M tert-butyllithium in pentane are added dropwise. The mixture is stirred at −78° C. for 1 hour and, after addition of 518 mg (2.9 mmol) of 3-isopropyl-4-methoxybenzaldehyde dissolved in 1 ml of ether/cyclohexane (1/1), stirred at −78° C. for 30 min and at room temperature for one hour. It is diluted with water and ether, the organic phase is washed with 10% strength citric acid solution, sodium bicarbonate solution and water and dried over sodium sulphate, and the solvent is removed in vacuo. Purification by chromatography (cyclohexane/ethyl acetate=9:1) affords 0.76 g (53%) of tert-butyl 4-[hydroxy(4-methoxy-3-isopropylphenyl)methyl]-3,5-dimethylphenylcarbamate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06803480B2
出典データセットuspto-grants-2004_10
ORD IDord-39b626e8ea814c1fb5335a2e62d1f4d6
出典メモuspto-grants-2004_10