Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thionyl Chloride → N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 2-Amino-5-methoxyphenol | HCID 9942163 | — |
| 반응물 | 2-Bromo-5-methylthiophene-3-carboxylic acid | HCID 11117589 | — |
| 반응물 | 2-Bromo-5-methyl-3-thiophenecarbonyl chloride | HCID 18422254 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamide | HCID 10860794 | 56.5% |
반응 단계
2-Bromo-5-methyl-3-thiophenecarbonyl chloride (2.6 g), prepared in the same manner as above from 2-bromo-5-methyl-3-thiophenecarboxylic acid and thionyl chloride, was suspended in toluene (20 ml). This toluene solution was added dropwise to a solution of 2-amino-5-methoxyphenol (2.0 g) in pyridine (50 ml) at 0° C. The mixture was stirred at room temperature for 2.5 hours and the solvent was evaporated under reduced pressure. The precipitated crystals were collected by filtration, and washed with diluted hydrochloric acid and diisopropyl ether to give N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamide (2.1 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06271225B1 |
| 출처 데이터셋 | uspto-grants-2001_08 |
| ORD ID | ord-1c94d5856e89420f893e5855ffbaf56d |
| 출처 메모 | uspto-grants-2001_08 |