Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium hydride → tert-Butyl 4-cyano-4-(2-methylphenyl)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-(o-Tolyl)acetonitrile | HCID 31155 | — |
| 반응물 | N-BOC-N,N-Bis(2-chloroethyl)amine | HCID 11230235 | — |
| 용매 | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| 생성물 | tert-Butyl 4-cyano-4-(2-methylphenyl)piperidine-1-carboxylate | HCID 22625983 | — |
반응 단계
A solution of bis(2-chloroethyl)-N-(1,1-dimethylethoxy)carbonyl amine (1.438 g, 5.94 mmol) and 2-methylphenyl acetonitrile (600 mg, 3.96 mmol) in a 4:1 mixture of THF/DMF (15 mL) was treated with NaH (357.9 mg, 8.7 mmol) at 60° C. (3 d). The solvent was removed in vacuo, the residue dissolved in EtOAc (200 ml) and washed with saturated NaHCO3 (50 ml), H2O (2×50 ml), and saturated aqueous NaCl (50 ml), dried (Na2SO4) and concentrated in vacuo. PCTLC (SiO2, 6 mm, 100% hexane) afforded 4-cyano-N-(1,1-dimethylethoxy)carbonyl-4-(2-methylphenyl) piperidine as a yellow/orange oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06274583B1 |
| 출처 데이터셋 | uspto-grants-2001_08 |
| ORD ID | ord-47a2f0d30788418ca2bdd90ab93eaf59 |
| 출처 메모 | uspto-grants-2001_08 |