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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1698753생성일: 2026년 10월 26일

Water → 135367-08-7

https://huagongshe.com/reaction/1698753

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorosuccinimideHCID 31398—
반응물Potassium BromideHCID 253877—
반응물2beta-Carbomethoxy-3beta-(4-trimethylsilylphenyl)tropaneHCID 69736376—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매Diethyl EtherHCID 3283—
생성물135367-08-7HCID 57340111100.3%

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온도60 °C

반응 단계

A mixture of 2β-Carbomethoxy-3β-(4′-trimethylsilylphenyl)tropane (594 mg, 1.79 mmol) and KBr (320 mg, 2.68 mmol) in 15 mL of acetic acid and 2 mL of MeOH was stirred at 60° C. for 20 min. 285 mg of NCS (2.15 mmol) was added at one time and the resulting mixture was stirred at the same temperature for 4 hrs. After cooling to rt 100 mL of H2O and 50 mL of Et2O were added. The aqueous phase was separated and the organic phase was extracted with 3N HCl (20 mL). The combined aqueous phase was washed with 20 mL of Et2O, basified with concentrated NH4OH and extracted with CH2Cl2 (2×50 mL). The solution was then dried and the removal of the solvent in vacuo gave the pure product as a white solid (607 mg, 100%). m.p. 114-116° C. 1H NMR (CDCl3, 400 MHz) δ 7.38 (d, J=8.4 Hz, 2H), 7.13 (d, J=8.4 Hz, 1H), 3.58-3.55 (m, 1H), 3.51 (s, 3H), 3.38-3.36 (m, 1H), 2.98-2.86 (m, 2H), 2.56 (dt, J−12.8, 2.8 Hz, 1H), 2.23 (s, 3H), 2.26.2.05 (m, 2H), 1.75-1.58 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06344179B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-a43917e772484797aa478e2e62be5eda
출처 메모uspto-grants-2002_02