참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Isopropyl-4-methoxybenzaldehyde | HCID 9898990 | — |
| 반응물 | tert-Butyl (4-bromo-3,5-dimethylphenyl)carbamate | HCID 22662122 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 반응물 | HCID 178418348 | HCID 178418348 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Pentane | HCID 8003 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 용매 | Cyclohexane diethylether | HCID 21895417 | — |
| 생성물 | HCID 22662124 | HCID 22662124 | 65.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06803480B2 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-39b626e8ea814c1fb5335a2e62d1f4d6 |
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| 출처 메모 | uspto-grants-2004_10 |
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