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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251473생성일: 2026년 10월 27일

1-Chloroethyl chloroformate → Hydrochloric Acid

https://huagongshe.com/reaction/251473

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참여 물질

역할이름HCID투입량
반응물1-Chloroethyl chloroformateHCID 521305—
반응물1'-Benzyl-3H-spiro[isobenzofuran-1,4'-piperidin]-3-oneHCID 10266406—
용매DichloromethaneHCID 6344—
생성물Hydrochloric AcidHCID 313484%
생성물3H-spiro(isobenzofuran-1,4'-piperidin)-3-oneHCID 9834255—

반응 조건

온도25 °C

반응 단계

To a solution of 1′-benzyl-3H-spiro[isobenzofuran-1,4′-piperidin]-3-one 1b (6 g, 20.4 mmol) in dichloromethane (30 mL) was added dropwise 1-chloroethyl chloroformate (2.9 g, 20.4 mmol). The mixture was stirred at 25° C. for 5 hr and then was concentrated to dryness under reduced pressure. The residue was dissolved in methanol and the mixture was heated to reflux for 30 min. The mixture was concentrated to dryness and ether was added. The precipitated solid was collected by filtration and washed with ether, dried in air to obtain 3H-spiro[isobenzofuran-1,4′-piperidin]-3-one 1c as its HCl salt (3.6 g). 1H-NMR (400 MHz, DMSO-d6) δ 9.16 (br, 2H), 7.86-7.81 (m, 2H), 7.63 (t, J=7.6 Hz, 1H), 7.56 (d, J=7.2 Hz, 1H), 3.39-3.42 (m, 2H), 3.11-3.14 (m, 2H), 2.47-2.48 (m, 2H), 1.85 (d, J=14.4 Hz, 2H). MS (ESI) m/z (M+H+): 203.24.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863449B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-89918feb11fd4c38bf5b490d6eb41b76
출처 메모uspto-grants-2011_01