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Ethanol → 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 反応物 | 1-Benzhydryl-3-(2-(thiophen-2-yl)ethoxy)azetidine | HCID 67154539 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride hydrochloride | HCID 67154553 | — |
反応手順
1-Chloroethylchloroformate (361 μL, 3.33 mmol) was added to a solution of 1-benzhydryl-3-(2-(thiophen-2-yl)ethoxy)azetidine (1.11 g, 3.17 mmol) in dichloromethane (15 mL) at room temperature. The reaction mixture was stirred overnight at room temperature, then 1 hour at 70° C. After cooling down to room temperature, ethanol (15 mL) was added and the reaction mixture was stirred at 70° C. for 1 hour. After concentration to dryness, the crude mixture was triturated in pentane (2×15 mL) to give a yellow oil (698 mg, quantitative) which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09321769B2 |
| 出典データセット | uspto-grants-2016_04 |
| ORD ID | ord-493fa3e3df824bd49a8f8e3cd5759391 |
| 出典メモ | uspto-grants-2016_04 |