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(Ethoxycarbonylmethyl)triphenylphosphonium bromide → (5-Methylbenzofuran-2-yl)acetic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (Ethoxycarbonylmethyl)triphenylphosphonium bromide | HCID 73731 | — |
| 反応物 | 5-methyl-3H-benzofuran-2-one | HCID 10057646 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | (5-Methylbenzofuran-2-yl)acetic acid ethyl ester | HCID 70085569 | — |
反応手順
A mixture of the product of Step 2, above (56) (10.81 mmol) and (carbethoxymethyl)triphenylphosphonium bromide (12.0 mmol) in 50 ml of xylene was heated to 155° C. for 20 hours. The reaction was cooled to ambient temperature and concentrated to dryness. The crude residue was chromatographed on silica gel with gradient elution with 5% EtOAc in hexanes to 10% EtOAc in hexanes to obtain the title compound (57).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05789415 |
| 出典データセット | uspto-grants-1998_08 |
| ORD ID | ord-c08257b8fabf46059237a9ce479172fe |
| 出典メモ | uspto-grants-1998_08 |