참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Lithium formate | HCID 23680280 | — |
| 반응물 | 2,4-Di-tert-butylphenyl methanesulfonate | HCID 44542716 | — |
| 촉매 | HCID 178418390 | HCID 178418390 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1,3-Di-tert-butylbenzene | HCID 136810 | 99.7% |
반응 단계
In a nitrogen atmosphere under normal pressure, 2,4-di-tert-butylphenyl methanesulfonate (500 g, 1.76 mols), lithium formate (183 g, 3.52 mols) and methanol (3000 g) were mixed at 25° C., and with stirring, 10 mass % Pd/carbon (50 mass % water-containing product) (100 g) (as metal palladium; 1 mass % relative to 2,4-di-tert-butylphenyl methanesulfonate) as supported by a carbon carrier having a specific surface area of 780 m2/g (by BET method) was put into it. With stirring, the reaction liquid was reacted at the same temperature for 4 hours. Water (100 mL) was added to the reaction liquid and Pd-carbon was separated through filtration, then heptane (500 g) was added to the filtrate. The organic layer obtained after extraction was concentrated under reduced pressure to give crude 1,3-di-tert-butylbenzene (334 g, yield 100% by mass).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08283508B2 |
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| 출처 데이터셋 | uspto-grants-2012_10 |
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| ORD ID | ord-016669ea2bd44e0b8a3f68feac687b37 |
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| 출처 메모 | uspto-grants-2012_10 |
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