関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triisopropyl borate | HCID 21531 | — |
| 反応物 | 6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene | HCID 10586063 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid | HCID 22571498 | — |
反応手順
To a cold (−78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6 M in hexane) of n-BuLi. The resulting solution was stirred at −78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06855832B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-1d3460c5657a46a1b80f064616bcbac3 |
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| 出典メモ | uspto-grants-2005_02 |
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