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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392886생성일: 2026년 10월 24일

3-Isopropyl-4-methoxybenzaldehyde → HCID 22662124, 화합물

https://huagongshe.com/ko/reaction/392886

반응식

참여 물질

역할이름HCID투입량
반응물3-Isopropyl-4-methoxybenzaldehydeHCID 9898990—
반응물tert-Butyl (4-bromo-3,5-dimethylphenyl)carbamateHCID 22662122—
반응물HCID 178418306HCID 178418306—
반응물HCID 178418348HCID 178418348—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
용매CyclohexaneHCID 8078—
용매Cyclohexane diethyletherHCID 21895417—
생성물HCID 22662124HCID 2266212465.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06803480B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-39b626e8ea814c1fb5335a2e62d1f4d6
출처 메모uspto-grants-2004_10