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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1197687생성일: 2026년 10월 26일

Benzyl isocyanate → N-(6-Cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)-N'-(phenylmethyl)urea

https://huagongshe.com/reaction/1197687

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl isocyanateHCID 76639—
반응물N-(6-Cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)-N'-phenylureaHCID 9973362—
용매EthanolHCID 702—
생성물N-(6-Cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)-N'-(phenylmethyl)ureaHCID 1529555785.7%

반응 단계

A solution of the title D compound from Example 8 (0.50 g, 2.47 mmoles) and benzyl isocyanate (0.33 g, 2.47 mmoles) in anhydrous ethanol (4 ml) was heated at reflux for 3 hours and cooled to room temperature. The reaction product precipitated from solution. It was collected by suction filtration; the solid was triturated with diisopropyl ether and dried under vacuum to obtain 0.71 g of the title compound as a white solid, m.p. 168-169° C. 1H NMR (DMSO-d6) δ 7.59 (s, 1 H), 7.56 (s, 1 H), 7.38-7.24 (m, 5 H) 6.89 (d, J=8.21 Hz, 1 H), 6.56 (t, J=5.87 Hz, 1 H), 6.50 (d, J=8.21 Hz, 1 H), 4.94 (M, 1 H), 4.30 (d, J=5.86 Hz, 2 H), 2.10 (m, 1 H), 1.74 (m, 1 H), 1.41 (s, 3 H), 1.28 (s, 3 H). 13C NMR (DMSO-d6) δ 158.11, 157.19, 140.78, 132.25, 132.08, 128.22, 126.93, 126.61, 126.12, 119.18, 118.03, 102.02, 77.28, 43.01, 41.95, 38.81, 29.08, 24.42.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05276168
출처 데이터셋uspto-grants-1994_01
ORD IDord-bc133ca288eb4053aaf03352a0267cdc
출처 메모uspto-grants-1994_01