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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2281755생성일: 2026년 10월 25일

Acetic Acid → 1-(4-Ethynylphenyl)pyrrolidine

https://huagongshe.com/reaction/2281755

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PyrrolidineHCID 31268—
반응물4-EthynylbenzaldehydeHCID 2771645—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물1-(4-Ethynylphenyl)pyrrolidineHCID 85899440—

반응 단계

Glacial acetic acid (0.2 mL) was added to a mixture of 4-ethynylbenzaldehyde (1 g, 7.5 mmol), pyrrolidine (1.2 mL, 15 mmol) and NaBH(OAc)3 (2.5 g, 11.5 mmol) in DCE (35 mL). The resulting mixture was stirred for 2 h at rt. The reaction was quenched with saturated aqueous NaHCO3 (50 mL). The product was extracted into CH2Cl2 (2×100 mL), and the combined organic layer was washed with brine (25 mL), dried (MgSO4) and evaporated in vacuo to give 1-(4-ethynylphenyl)pyrrolidine in quantitative yield. 1H NMR (CDCl3) δ: 7.45 (d, J=7.8 Hz, 2H), 7.30 (d, J=8.3 Hz, 2H), 3.62 (s, 2H), 3.06 (s, 1H), 2.51 (bs, 4H), 1.80 (bs, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09139563B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-616926857ab841578b38598b1e134f67
출처 메모uspto-grants-2015_09