Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → N-Nitrosodiphenylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | N,N-Diphenylhydrazine | HCID 10739 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-Nitrosodiphenylamine | HCID 6838 | — |
반응 단계
The compound 1,1-diphenylhydrazine is commercially available. The substituted 1,1-diphenylhydrazines can be made by reacting the corresponding 1,1-diarylamine with sodium nitrite and hydrochloric acid in dimethylformamide at about 10° C. to produce an N-nitrosodiphenylamine, then adding the N-nitroso compound in tetrahydrofuran to a suspension of lithium aluminum hydride in dry ether under nitrogen and maintaining the temperature at 25°-35° C. for about 11/2 hours. The procedure is analogous to that given for preparation of N-amino-iminodibenzyl in Cohen et al., U.S. Pat. No. 3,457,271.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04174453 |
| 출처 데이터셋 | uspto-grants-1979_11 |
| ORD ID | ord-0c3fb338056e45c39b026fdfa6162000 |
| 출처 메모 | uspto-grants-1979_11 |