참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia;borane | HCID 419330 | — |
| 반응물 | 3,5-dinitro-1H-1,2,4-triazole | HCID 3283598 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 생성물 | ammonium tetrakis(3,5-dinitro-1H-1,2,4-triazolyl)borate | HCID 131735309 | — |
반응 단계
A 150 mL glass ampule equipped with a grease free high-vacuum PTFE valve and a TEFLON™ coated stir bar was flamed-out under vacuum. Inside the dry-box, the ampule was loaded with 1.18 g (8.00 mmol) 3,5-dinitro-1H-1,2,4-triazole and 61.6 mg (2.00 mmol) ammonia borane. The ampule was connected to a vacuum line, evacuated and cooled to −196° C. About 10 mL of dry dimethoxyethane was slowly condensed into the ampule. The ampule was closed and allowed to warm to ambient temperature. After 30 minutes, the ampule was heated to 110° C. for eight hours. The obtained yellow solution was cooled to −196° C. and 5.9 mmol of evolved hydrogen was pumped off. The reaction mixture was allowed to warm to ambient temperature. Subsequent evacuation to a constant weight over 24 hours resulted in a yellow solid of ammonium tetrakis(3,5-dinitro-1H-1,2,4-triazolyl)borate, 8.0 mmol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09309266B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-c997c99103954c89aa5d9e746257d31c |
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| 출처 메모 | uspto-grants-2016_04 |
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