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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269135생성일: 2026년 10월 25일

Acetyl chloride → Tert-butyl 4-[3-(acetylamino)phenyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1269135

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물TriethylamineHCID 8471—
반응물tert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylateHCID 22049268—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-[3-(acetylamino)phenyl]-1-piperidinecarboxylateHCID 2204942299%

반응 단계

Into a solution of 14.6 g (52.6 mmol) of tert-butyl 4-[3-(amino)phenyl]-1-piperidinecarboxylate and 14.7 mL (105 mmol) of triethylamine in 120 mL THF at 0° C. was slowly added 4.5 mL (63.1 mmol) of acetyl chloride. The reaction mixture was stirred at room temperature for 2 hours and concentrated in vacuo. The residue was dissolved in CH2Cl2 and washed with H2O, followed by brine. The organic layer was dried over MgSO4 and concentrated in vacuo to give 16.6 g (52.1 mmol, 99%) of desired product: 1H NMR (400 MHz, CDCl3) δ 7.41–7.20 (m, 3H), 6.94 (d, 1H, J=7.5 Hz), 4.21 (m, 2H), 2.75 (m, 2H), 2.62 (m, 1H), 2.16 (s, 3H), 1.78 (m, 2H), 1.56 (m, 2H), 1.48 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199135B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-41d8044313374353b9cca9cc3c3e93f1
출처 메모uspto-grants-2007_04