참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | (2-Bromophenyl)(2,4,6-trimethoxybenzyl)sulfane | HCID 66870845 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(2,4,6-Trimethoxybenzylthio)phenylboronic acid | HCID 68643617 | 46% |
반응 단계
To a solution of 4.22 g (2-bromophenyl)(2,4,6-trimethoxybenzyl)sulfane (11.56 mmol) in 150 ml dry THF at −78° C. was added slowly 5.6 ml 2.5M n-BuLi. The solution was stirred at −78° C. for 25 minutes. 1.6 ml B(OMe)3 was added at −78° C. The reaction was stirred 2 hours at RT. 100 ml water was added, stirred overnight. The mixture was extracted with ethyl acetate (2×100 ml). The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by gradient chromatography (hexane:ethyl acetate 60:40) yielded 1.762 g product (5.3 mmol, 46% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07550505B2 |
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| 출처 데이터셋 | uspto-grants-2009_06 |
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| ORD ID | ord-5bb9f67d1d0041ea82ea67177f16ec95 |
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| 출처 메모 | uspto-grants-2009_06 |
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