참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Trifluoroacetohydrazide | HCID 229753 | — |
| 반응물 | 4,4,4-Trinitrobutyryl chloride | HCID 12507556 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | N-(4,4,4-trinitrobutyryl)-N'-(trifluoroacetyl)hydrazine | HCID 19738490 | — |
반응 단계
To 1.65 g (0.007 mole) of 4,4,4-trinitrobutyryl chloride in 15 mL of anhydrous diethyl ether stirred in a water bath at 15° C. was added 0.9 g (0.007 mole) of N-(trifluoroacetyl)hydrazine. Pyridine (0.6 mL, 0.007 mole) was added dropwise. After 3 minutes, dilute hydrochloric acid was added and the ether layer was separated and dried (Na2SO4). The volatiles were removed and the residue was stirred with water and then with CH2Cl2 to give the product N-(4,4,4-trinitrobutyryl)-N'-(trifluoroacetyl)hydrazine, 1.15 g (50%), mp 154°-156° C. Crystallization from 1,2-dichloroethane raised the melting point to 157°-159° C.; 1H NMR (acetone-d6 +D2O): 2.97 (t, 2H), 3.86 (t, 2H); IR (KBr): 3330, 3220 (NH), 1745, 1690 (C=O); 1610, 1590 (NO2); 1195 (C--F).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05241071 |
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| 출처 데이터셋 | uspto-grants-1993_08 |
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| ORD ID | ord-cd6378f167c343a8b51d4310fdf8df54 |
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| 출처 메모 | uspto-grants-1993_08 |
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