Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | — |
| 반응물 | methyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamate | HCID 19042327 | — |
| 촉매 | Potassium Iodide | HCID 4875 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate | HCID 15766845 | 93.1% |
반응 단계
Methyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamate (1.64 Kg, 7.47 mol), cyclopentyl-p-toluenesulfonate (1.80 Kg, 7.48 mol), potassium carbonate (1.03 Kg, 7.46 mol) and potassium iodide (12.3 g, 1.0 mol %) were placed in a 10L three-necked flask equipped with a stirrer and a Dimroth funnel, and, after adding acetone (7.5 liters) as a solvent thereto, the mixture was refluxed under heating for4 hours. After completion of the reaction, the reaction solution was taken out, and 0.5N hydrochloric acid (20 liters) was added thereto while vigorously stirring. The precipitated methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate as a white solid (2.0 Kg, 6.95 mol, 93.1% yield) was isolated by filtration and thoroughly dired.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05554581 |
| 출처 데이터셋 | uspto-grants-1996_09 |
| ORD ID | ord-2a4e3ab8cf6c471282fa64238545f162 |
| 출처 메모 | uspto-grants-1996_09 |