참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzene | HCID 23080940 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,6-Dimethoxy-4-methoxymethylphenylboric acid | HCID 23080945 | — |
반응 단계
n-Butyllithium (2.64M hexane solution; 182 mL) was added dropwise to a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (121.3 g) in tetrahydrofuran (730 mL) at −78° C., and the mixture was stirred for 20 minutes. A solution of trimethoxyborane (61.7 mL) in tetrahydrofuran (20 mL) was then added to the reaction mixture at −78° C. When internal temperature was raised to −10° C., to the reaction mixture was added saturated aqueous ammonium chloride (730 mL), and stirring was continued for 15 minutes. The obtained reaction mixture was extracted with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (90.4 g) was obtained as a white solid from the n-hexane:ethyl acetate (2:3) fraction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07176216B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-98cd5e7682ec4cf5b59bbbfda0652f27 |
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| 출처 메모 | uspto-grants-2007_02 |
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