Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1674721생성일: 2026년 10월 24일
1-Phenethylamine, (-)- → (S)-tert-butyl 4-(1-phenylethylimino)-3,4-dihydro-2H-spiro[naphthalene-1,4'-piperidine]-1'-carboxylate
https://huagongshe.com/ko/reaction/1674721
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Phenethylamine, (-)- | HCID 75818 | — |
| 반응물 | Tert-butyl 4-oxo-3,4-dihydro-2H-spiro[naphthalene-1,4'-piperidine]-1'-carboxylate | HCID 49760950 | — |
| 반응물 | HCID 178494437 | HCID 178494437 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (S)-tert-butyl 4-(1-phenylethylimino)-3,4-dihydro-2H-spiro[naphthalene-1,4'-piperidine]-1'-carboxylate | HCID 58033911 | — |
반응 단계
A solution of tert-butyl 4-oxo-3,4-dihydro-2H-spiro[naphthalene-1,4′-piperidine]-1′-carboxylate (A4) (5.0 g, 15.8 mmol), (S)-1-phenylethanamine (3.0 ml, 23.8 mmol) and boron trifluoride dimethyl etherate (0.5 ml, 5 mmol) in dry toluene (150 ml) was heated at 140° C. under a Dean-Stark trap for 24 hours. The solvent was distilled and the residue was cooled with an ice bath, dissolved in ethyl acetate, washed with saturated NaHCO3, and water. The organic phase was dried over Na2SO4, filtered and concentrated to give (S)-tert -butyl 4-(1-phenylethylimino)-3,4-dihydro-2H-spiro[naphthalene-1,4′-piperidine]-1′-carboxylate (B1) as a gum. LC-MS analysis of the crude indicated that there is trace of starting material (A4). LC-MS: m/e=419.37 (M+H). Rt=2.24 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08003660B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-9a96c496ad524adc967620bd1c93e6c4 |
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| 출처 메모 | uspto-grants-2011_08 |
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