Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hexane → 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene | HCID 12985690 | — |
| 촉매 | Iron | HCID 23925 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine | HCID 12985691 | — |
반응 단계
To a refluxing well-stirred suspension of iron powder (19.6 g, 100 mesh) in ethanol (60 mL), water (13.4 mL) and 36% hydrochloric acid (1.4 mL) was added 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene (24 g) in portions over 15-30 minutes. After 3 hours thin-layer chromatography (TLC) (ethyl acetate:hexane, 40:60) showed no substrate. The reaction mixture was then filtered hot and the iron oxide filter cake was washed with hot ethanol. The combined ethanol washes were evaporated to produce a residue. The residue was taken up in diethyl ether, washed with aqueous bicarbonate and water, dried (MgSO4), filtered, and evaporated, to give 4-chloro-3-(3-methyl-2-butenyloxy)benzenamine, 19.8 g of light brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06710077B1 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-c4e4019637dc499c97aa04611feb8ff6 |
| 출처 메모 | uspto-grants-2004_03 |