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5-Fluoro-2-nitrophenol → tert-Butyl 2-(5-fluoro-2-nitrophenoxy)propylcarbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Fluoro-2-nitrophenol | HCID 9937 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| 反応物 | tert-butyl N-(2-hydroxypropyl)carbamate | HCID 9920508 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | tert-Butyl 2-(5-fluoro-2-nitrophenoxy)propylcarbamate | HCID 58413346 | — |
反応手順
2-Nitro-5-fluorophenol (3.0 g) and tert-butyl-N-(2-hydroxypropyl)carbamate were dissolved in THF (20 ml) and triphenylphosphine (7.5 g) and di-tert-butyl-azodicarboxylate were added. The exothermic reaction was cooled in an ice bath. Then the reaction mixture was stirred at room temperature for 2 h. The mixture was concentrated in vacuo and the residue was purified by chromatography (silica gel/dichloromethane: petroleum ether 1:2). The fractions were combined and concentrated in vacuo. The residue was dissolved in dichloromethane and washed with 1M NaOH. The organic layer was separated, dried, filtered and concentrated in vacuo.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08853193B2 |
| 出典データセット | uspto-grants-2014_10 |
| ORD ID | ord-a54366de612342b5a3f8b964f31e818d |
| 出典メモ | uspto-grants-2014_10 |