Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Phthalic Anhydride → HCID 131718923, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Phthalic Anhydride | HCID 6811 | — |
| 반응물 | 6-Aminonaphthalene-1-sulphonic acid | HCID 66470 | — |
| 반응물 | Triethylammonium | HCID 1385867 | — |
| 반응물 | Sodium 6-aminonaphthalene-1-sulphonate | HCID 23696805 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | HCID 131718923 | HCID 131718923 | — |
반응 단계
223 g (1 mol) of 6-amino-1-naphthalenesulfonic acid and 148 g (1 mol) of phthalic anhydride are boiled for 0.5 h in 1 liter of pyridine. After boiling, the reaction mixture is left at room temperature for 16 h. The precipitated product is filtered and washed with pyridine and water, and then recrystallized from boiling water. Yield 298 g (69%); mp 234°-237° C.; Anal. Calcd. for C23H16N2SO5 :C 63.88, H 3.73, N 6.48, S 7.42; Found:C 63.74, H 3.81, N 6.52, S 6.99. When the 6-phthalimido-1-naphthalenesulfonic acid pyridinium salt was synthesized starting from 6-amino-1-naphthalenesulfonic acid sodium salt or triethylammonium salt, the calculated yields were 63% and 58% respectively.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05399487 |
| 출처 데이터셋 | uspto-grants-1995_03 |
| ORD ID | ord-05251847db624057a3846b096fcc6b76 |
| 출처 메모 | uspto-grants-1995_03 |