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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

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenethylamine, (-)-HCID 75818—
반응물Tert-butyl 4-oxo-3,4-dihydro-2H-spiro[naphthalene-1,4'-piperidine]-1'-carboxylateHCID 49760950—
반응물HCID 178494437HCID 178494437—
용매TolueneHCID 1140—
생성물(S)-tert-butyl 4-(1-phenylethylimino)-3,4-dihydro-2H-spiro[naphthalene-1,4'-piperidine]-1'-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003660B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-9a96c496ad524adc967620bd1c93e6c4
출처 메모uspto-grants-2011_08