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Triethylamine → 1,3-Bis(2-ethoxycarbonylethylthio)acetone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,3-Dichloroacetone | HCID 10793 | — |
| 反応物 | Ethyl 3-mercaptopropionate | HCID 21625 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,3-Bis(2-ethoxycarbonylethylthio)acetone | HCID 15885283 | 99.9% |
反応手順
To a stirred solution of 1,3-dichloroacetone (6.85 g, 54 mmol) and ethyl 3-mercaptopropionate (13.9 mL, 108 mmol) in anhydrous tetrahydrofuran (150 mL) was dropwise added triethylamine (15.0 mL, 108 mmol) at 0° C. and stirred at room temperature for 24 h. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The ethyl acetate phase was washed with 5% hydrochloric acid and then brine, dried over sodium sulfate, and concentrated to dryness, affording 17.4 g of the crude 1,3-bis(2-ethoxycarbonylethylthio)acetone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05859256 |
| 出典データセット | uspto-grants-1999_01 |
| ORD ID | ord-c0f6a0bfe87443ebbc95c2d6994bc16f |
| 出典メモ | uspto-grants-1999_01 |