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Morpholine → N-(2-methoxy-6-nitrophenyl)-2-morpholin-4-ylacetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 2-bromo-N-(2-methoxy-6-nitrophenyl)acetamide | HCID 57436027 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-(2-methoxy-6-nitrophenyl)-2-morpholin-4-ylacetamide | HCID 57436028 | 75.6% |
反応手順
To a solution of 2-bromo-N-(2-methoxy-6-nitrophenyl)acetamide (Step 1, 8.8 g, 30 mmol) in THF (240 mL) was added morpholin (11 mL, 122 mmol) at 0° C. and warmed to rt. After 2.5 h, the reaction mixture was quenched by addition of water (200 mL) and extracted with ethyl acetate (200 mL×2). The combined organic layers were washed with water (200 mL), brine (100 mL) dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (2/1) to afford 6.7 g (75%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08138177B2 |
| 出典データセット | uspto-grants-2012_03 |
| ORD ID | ord-184fbfc0ca2f49c98231e4027798ca7a |
| 出典メモ | uspto-grants-2012_03 |