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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1173004생성일: 2026년 10월 26일

Water → HCID 11371354, 화합물

https://huagongshe.com/reaction/1173004

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Pyridin-2-ylbenzaldehydeHCID 1515240—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(1R,2R)-2-(4-aminophenyl)cyclopropane-1-carboxylic acidHCID 68668314—
용매DichloromethaneHCID 6344—
용매1,1-DichloroethaneHCID 6365—
생성물HCID 11371354HCID 1137135422.3%

반응 단계

A suspension of racemic-(trans)-2-(4-aminophenyl)cyclopropanecarboxylic acid (I-1) (0.30 g, 1.69 mmol) and 4-(2-pyridinyl)benzaldehyde (0.37 g, 2.03 mmol) in dichloroethane (10 mL) were heated to reflux until a clear solution formed. The solution was cooled to RT then NaB(OAc)3H (0.54 g, 2.54 mmol) was added and stirred for 2 h. Water (50 mL) and dichloromethane (50 mL) were added and the organic layer was separated, dried over Na2SO4, filtered and concentrated. The crude material was purified on silica gel eluting with an increasing gradient from 20% ethyl acetate/hexanes to 100% ethyl acetate to give the title compound as a white solid (0.13 g, 22%). 1H NMR (400 MHz, DMSO) δ 12.15 (s, 1H), 8.65 (d, J=4.1 Hz, 1H), 8.02 (d, J=8.3 Hz, 2H), 7.92 (d, J=8.2 Hz, 1H), 7.86 (t, J=8.0 Hz, 1H), 7.44 (d, J=8.1 Hz, 2H), 7.32 (dd, J=5.2, 6.6 Hz, 1H), 6.84 (d, J=8.4 Hz, 2H), 6.50 (d, J=8.4 Hz, 2H), 6.23 (s, 1H), 4.30 (d, J=4.6 Hz, 2H), 2.22-2.17 (m, 1H), 1.61-1.57 (m, 1H), 1.31-1.27 (m, 1H), 1.20-1.16 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834013B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-275249f37c294cbe8130317dc07d1488
출처 메모uspto-grants-2010_11