Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → Tert-butyl 4-(4-formylphenyl)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethylsilane | HCID 68337 | — |
| 반응물 | Tert-butyl 4-[4-(methoxycarbonyl)phenyl]-1-piperidinecarboxylate | HCID 22492933 | — |
| 촉매 | Chlorobis(cyclooctene)iridium(I) dimer | HCID 91972094 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Tert-butyl 4-(4-formylphenyl)piperidine-1-carboxylate | HCID 11254770 | — |
반응 단계
To a solution of 4-(4-methoxycarbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (776 mg, 2.43 mmol) in dichloromethane (10 ml) are added diethylsilane (470 μl, 3.64 mmol) and chlorobis(cyclooctene)iridium(I) dimer (22 mg, 0.025 mmol) and the mixture is irradiated in a microwave reactor for 1.5 hours at 50° C. The reaction mixture is stirred vigorously with 2 N hydrochloric acid (0.6 ml) for 30 minutes. The organic layer is separated, dried over sodium sulfate and evaporated. The residue is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent to afford 4-(4-formyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester as yellow resin; HPLC/MS 2.10 min (A), [M-tBu] 234.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09388142B2 |
| 출처 데이터셋 | uspto-grants-2016_07 |
| ORD ID | ord-a2d39eaebcff4592a102c56034108187 |
| 출처 메모 | uspto-grants-2016_07 |