Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → Tert-butyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Borohydride | HCID 28123 | — |
| 반응물 | Tert-butyl 4-[(tert-butoxycarbonyl)hydrazono]piperidine-1-carboxylate | HCID 20824233 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Tert-butyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylate | HCID 20824232 | — |
반응 단계
150 ml of a solution of borohydride in tertahydrofurane (1.0 mol/l) is slowly added to a solution of 0.12 mole of 4-(tert-Butoxycarbonyl-hydrazono)-piperidine-1-carboxylic acid tert-butyl ester (intermediate product A9) in 100 ml of dry tetrahydrofurane. After complete addition, the mixture is stirred for another 30 min after which a 100 ml of water is added to destroy the excess of borohydride. Subsequently the tetrahydrofurane is evaporated and the resulting aqeous solution extracted with diethyl ether. After drying the solvent over magnesium sulfate, the ether is evaporated. M. p.112–115° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07186710B2 |
| 출처 데이터셋 | uspto-grants-2007_03 |
| ORD ID | ord-58a1a318dffc4f008fe79b3a93bb6e97 |
| 출처 메모 | uspto-grants-2007_03 |