참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | Benzenemethanamine, 3-bromo- | HCID 457587 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 반응물 | HCID 178418348 | HCID 178418348 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [3-(Methylamino)phenyl]boronic acid | HCID 23558980 | 40% |
반응 단계
37.6 g (202 mmol, 1 eq) of (3-bromophenyl)methylamine (obtained as in 1c) are dissolved in 300 mL of tetrahydrofuran. The reaction mixture is cooled to −70° C. and 166 mL (242 mmol, 1.2 eq) of 1.5 M methyllithium are then added slowly, while keeping the temperature at −70° C. The reaction mixture is stirred for 1 hour at −70° C. 306 mL (444 mmol, 2.2 eq) of 1.46 M tert-butyllithium are added, while keeping the temperature at −70° C. The reaction mixture is stirred for 45 minutes at −70° C. 103.5 ml (808 mmol, 4 eq) of trimethyl borate are added at −65° C. and the reaction mixture is then warmed to room temperature. The reaction is stopped by adding 1 L of 1 N hydrochloric acid. The pH is adjusted to pH 5 and the reaction medium is then extracted with n-butanol. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 11.3 g of N-methyl-3-aminophenylboronic acid are obtained. Yield=40%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08129416B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-f17f8fd4bde84d678656bf84f1aff273 |
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| 출처 메모 | uspto-grants-2012_03 |
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