참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 4-Chloro-2-ethoxybenzonitrile | HCID 22721189 | — |
| 생성물 | Ethyl 4-chloro-2-ethoxy-benzimidate hydrochloride | HCID 22996239 | 94% |
반응 단계
Hydrogen chloride gas was passed through a solution of 4-chloro-2-ethoxy-benzonitrile (670 mg, 3.689 mmol) in anhydrous ethanol (25 mL) cooled to 0° C. After 45 min, the hydrogen chloride gas was stopped and the reaction vessel was sealed with a Teflon stopper. It was stirred at room temperature for 5 d. The reaction vessel was cooled to 0° C. and the stopper was removed. The solvent was removed and the residue was triturated in diethyl ether to afford ethyl 4-chloro-2-ethoxy-benzimidate hydrochloride (913 mg, 94%). It was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06617346B1 |
|---|
| 출처 데이터셋 | uspto-grants-2003_09 |
|---|
| ORD ID | ord-2d3b6a1461914dc486337f5e277cdc85 |
|---|
| 출처 메모 | uspto-grants-2003_09 |
|---|