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Dicyclohexylcarbodiimide → Methyl 4-(bromomethyl)-3-nitrobenzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | 4-Bromomethyl-3-nitrobenzoic acid | HCID 132386 | — |
| 反応物 | 4-pyridinemethanamine, N,N-dimethyl- | HCID 264946 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Dichloromethane methanol | HCID 21226129 | — |
| 生成物 | Methyl 4-(bromomethyl)-3-nitrobenzoate | HCID 13399987 | — |
反応手順
A solution of dicyclohexylcarbodiimide (DCC, 0.95 g, 4.61 mmol, 1.2 equiv) in 10 mL of dichloromethane (DCM) was added dropwise to a stirred mixture of 4-bromomethyl-3-nitro-benzoic acid 1 (1.0 g, 3.84 mmol, 1.0 equiv) and 4-dimethylaminomethyl pyridine (DMAP) (0.020 g, 0.19 mmol, 0.05 equiv) in 10 mL of dichloromethane-methanol (10%) at room temperature. The mixture was stirred for 6 hours to obtain 4-bromomethyl-3-nitro-benzoic acid methyl ester 2. Dicyclohexyl urea (DCU) thus obtained was removed by filtration and the solvent in the filtered solution was removed under vacuum. The residue was purified by column chromatography using hexane-ethyl acetate (15%) as an eluant to give ester 2 as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08383662B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-ed0281c5bc0e43838b727eaf5f033ed9 |
| 出典メモ | uspto-grants-2013_02 |