Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,5-Dichlorobenzoic acid → 3-Chloro-6-(3,5-diisopropylphenoxy)benzoic Acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,5-Dichlorobenzoic acid | HCID 5784 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3,5-Bis(1-methylethyl)phenol | HCID 93104 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 3-Chloro-6-(3,5-diisopropylphenoxy)benzoic Acid | HCID 20298967 | 49.4% |
반응 단계
2,5-dichlorobenzoic acid (5 g) and 3,5-diisopropylphenol (4.66 g) were dissolved in dry xylene and the solution placed under dry oxygen-free nitrogen. Sodium hydride (1.25 g) was added as a suspension in petroleum ether. Cuprous bromide was added and the solution refluxed for 5 hours and cooled. The xylene was removed by low pressure distillation. The remaining solid was acidified with dilute hydrochloric acid and extracted with diethyl ether. The ethereal layer was separated, dried and distilled under low pressure to give an oil. The oil was dissolved in petroleum ether (30°-40° ). Standing gave a crystalline solid, which was recrystallised from hexane to give the title compound (4.3 g), mp 129°-130° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04242121 |
| 출처 데이터셋 | uspto-grants-1980_12 |
| ORD ID | ord-c41674c889ed47979e95692495323db8 |
| 출처 메모 | uspto-grants-1980_12 |