참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethanolamine | HCID 8113 | — |
| 반응물 | Butylboronic Acid | HCID 20479 | — |
| 반응물 | 2,3-Dihydroxy-N~1~,N~1~,N~4~,N~4~-tetramethylbutanediamide | HCID 6999257 | — |
| 반응물 | Dioxazaborocin | HCID 57497284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | 2-Butyl-1,3,6,2-dioxazaborocane | HCID 346607 | — |
반응 단계
2-(But-1-yl)-tetrahydro-4H-1,3,6,2-dioxazaborocine [CAS 92527-13-4] was prepared from n-butylboronic acid and 2-(2-hydroxy-ethylamino)-ethanol [CAS 111-42-2] as reported in Organic Synthesis, 1998, 76, 86-96. This dioxazaborocine (3 g, 17.5 mmol) and (2S,3S)-2,3-dihydroxy-N,N,N′,N′-tetramethyl-butanediamide [CAS 63126-52-3] (4.65 g) were dissolved in anhydrous dichloromethane (95 mL) under N2. Brine (30 mL) was added. The resulting mixture was stirred at room temperature for 1 hour. The two layers were separated, and the aqueous layer was extracted with dichloromethane (30 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide the title compound as an oil 1H NMR (300 MHz, CDCl3): δ 0.82-0.9 (m, 5H), 1.25-1.45 (m, 4H), 2.98 (s, 6H), 3.2 (s, 6H), 5.52 (s, 2H). MS (DCl—NH3) m/z 271 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08829041B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-d8d8b063e05b4152bcb42186af8a356e |
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| 출처 메모 | uspto-grants-2014_09 |
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