関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethylene Glycol | HCID 174 | — |
| 反応物 | Nitrogen | HCID 947 | — |
| 反応物 | Trimethyl orthoformate | HCID 9005 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3'-Bromoacetophenone | HCID 16502 | — |
| 生成物 | 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane | HCID 10999218 | — |
反応手順
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(3-bromo-phenyl)-ethanone (1360 mg, 6.83 mmol) in ethylene glycol (8.00 mL, 143.46 mmol) was treated with trimethylorthoformate (1.50 mL, 13.68 mmol) followed by LiBF4 (131 mg, 1.37 mmol). The reaction mixture was heated at 95° C. for 15 h. Sat. aq. Na2CO3 was added and the mixture was extracted twice with ether and the combined organic extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (10:1 hept-EA)=0.34. LC-MS-conditions 02: tR=1.01 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536209B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-2395729cc9094f8db19164bab0b1ef65 |
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| 出典メモ | uspto-grants-2013_09 |
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