Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzene → N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-(4-Benzylpiperazin-1-yl)aniline | HCID 737259 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide | HCID 960610 | 104.5% |
반응 단계
To a solution of 8.5 g (0.03 mol) of 4-[4-(phenylmethyl)-1-piperazinyl]benzeneamine and 16.0 g (0.16 mol) of triethylamine in 450 mL of ethyl acetate was added, dropwise, a solution of 2.5 g (0.035 mol) of acetyl chloride in 50 mL of ethyl acetate. The mixture was magnetically stirred for 3 h and then heated at reflux for 1 h. The excess acetyl chloride was co-distilled with benzene and the resulting oil was shaken in 400 mL of 10% sodium hydroxide solution. The suspended tan solid was collected by filtration, washed thrice with 100 mL portions of water, and air dried to give 9.7 g (99%) of crude product. A one-gram portion was recrystallized from benzene/petroleum ether to give 100 mg of cream colored solid, mp 159°-161° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05086055 |
| 출처 데이터셋 | uspto-grants-1992_02 |
| ORD ID | ord-b91b614deb55459cb6f1f80f11f2fd93 |
| 출처 메모 | uspto-grants-1992_02 |