참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | t-Butyl carbanilate | HCID 137930 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2-BOC-aminophenyl)boronic acid | HCID 2773226 | 53% |
반응 단계
To a cooled (-78° C.) solution of N-BOC aniline (5 g1 25.87 mmol) in THF (111.1 mL) was added tert-butyl lithium (38.9 mL, 66.7 mmol) and the mixture was stirred under an argon atmosphere for E5 min. It was then allowed to warm up to -20° C. and stirred at that temperature for 2 h. Trimethylborate was added (11.94 mL, 105.6 mmol) and the mixture was stirred until it warmed up to room temperature. Then, it was cooled to 0° C. and aqueous 10% HCl was added to pH=6.5. The layers were separated and the aqueous phase was extracted with CH2Cl2. The combined organic extracts were washed with brine, dried and concentrated to a crude product, which was washed with a mixture of EtOAc-hexane (5:95) to give the title compound as a yellow solid (53%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05827863 |
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| 출처 데이터셋 | uspto-grants-1998_10 |
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| ORD ID | ord-1fba30b2e7cb4f60822fb21c752f1138 |
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| 출처 메모 | uspto-grants-1998_10 |
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