化工社化工社 化学情報印刷レポート · 研究参考用
Diethanolamine → 2-Butyl-1,3,6,2-dioxazaborocane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethanolamine | HCID 8113 | — |
| 反応物 | Butylboronic Acid | HCID 20479 | — |
| 反応物 | N,N,N',N'-Tetramethyl-L-tartramide | HCID 6610750 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | 2-Butyl-1,3,6,2-dioxazaborocane | HCID 346607 | — |
反応手順
2-(But-1-yl)-tetrahydro-4H-1,3,6,2-dioxazaborocine [CAS 92527-13-4] (3 g, 17.5 mmol), which 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, and (2R,3R)-2,3-dihydroxy-N,N,N′,N′-tetramethyl-butanediamide [CAS 26549-65-5] (9.85 g) were dissolved in anhydrous dichloromethane (160 mL) under N2, Brine (25 mL) was added. The resulting mixture was stirred at room temperature for about 16 hours. The two layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with 50 mL brine, dried over MgSO4, filtered and concentrated in vacuo to provide the title compound as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829041B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-5e1ec3aea6574a1d88a733e20de2ceb7 |
| 出典メモ | uspto-grants-2014_09 |