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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1910482생성일: 2026년 10월 25일

1,2-Dichloroethane → 1,2-Diphenylethyl quinuclidine-3-carboxylate

https://huagongshe.com/reaction/1910482

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,2-DiphenylethanolHCID 94178—
반응물1-Azabicyclo(2.2.2)octane-3-carboxylic acid hydrochlorideHCID 12673436—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1,2-Diphenylethyl quinuclidine-3-carboxylateHCID 7092582553.3%

반응 단계

Quinuclidine-3-carboxylic acid hydrochloride (160 mg, 0.83 mmol), EDC (290 mg, 1.51 mmol), and HOBT (232 mg, 1.51 mmol) were dissolved in dry DMF (8 ml). 1,2-Diphenylethanol (150 mg, 0.76 mmol) and TEA (0.32 ml, 2.27 mmol) were added, and the resulting mixture was stirred at room temperature overnight. Then quinuclidine-3-carboxylic acid hydrochloride (72.5 mg, 0.38 mmol), EDC (87 mg, 0.45 mmol), and HOBT (57.9 mg, 0.38 mmol) were added followed by TEA (0.16 ml, 1.13 mmol), and the mixture was stirred for additional 32 hours. The mixture was diluted with water and extracted three times with Et2O. The organic phases were collected, washed with brine, dried over Na2SO4, filtered, and evaporated to dryness. The crude residue was purified by flash chromatography (DCM/MeOH=9/1) to obtain 1,2-diphenylethyl quinuclidine-3-carboxylate (136 mg, racemic mixture).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604015B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-687d831e5a4746f0b6410cf4c63f170c
출처 메모uspto-grants-2013_12