참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Bromophenol | HCID 7244 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2-Hydroxyphenyl)boronic acid | HCID 2773454 | 95.3% |
반응 단계
Part B: 2-Bromophenol (10.0 g, 57.8 mmol) was dissolved in dry THF (100 ml) in a dry 250 ml flask flushed with nitrogen. The mixture was chilled in a dry ice/2-propanol bath, n-butyl lithium (51 ml of a 2.5M solution in hexanes, 127.2 mmol) was added then the cooling bath was exchanged for an ice-water bath. The reaction was stirred for an hour at 0° C. then trimethyl borate (6.9 ml, 60.7 mmol) was added to the slurry which became homogeneous after a few minutes. The mixture was stirred at room temperature overnight then treated with 2N aqueous HCl to pH 3, mixed well for 30 minutes and extracted with ether (3×25 ml). The organic materials were combined, dried (MgSO4) then concentrated under reduced pressure which gave 7.6 g (91%) of 2-hydroxybenzeneboronic acid as a white solid, m.p. 156°-158° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05622937 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-bcdddbe9ef544c1db1c4749dadfff855 |
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| 출처 메모 | uspto-grants-1997_04 |
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