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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2218725생성일: 2026년 10월 27일

9,10-Dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-one → 4-(3,5-Dimethyl-benzylidene)-9,10-dihydro-4H-1-thia-benzo[f]azulene

https://huagongshe.com/reaction/2218725

반응식

참여 물질

역할이름HCID투입량
반응물9,10-Dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-oneHCID 768492—
반응물HCID 178424986HCID 178424986—
용매TetrahydrofuranHCID 8028—
생성물4-(3,5-Dimethyl-benzylidene)-9,10-dihydro-4H-1-thia-benzo[f]azuleneHCID 6893836657%

반응 단계

Following the procedures essentially as described in Example 238 and using 9,10-dihydro-1-thia-benzo[f]azulene-4-one (47.0 mg (0.22 mmol) and solution of 3,5-dimethylbenzyl magnesium bromide(0.650 mmol) in THF, provides, after dehydration, 39.6 mg (57%) of the title compound as a 1.6:1 mixture of E- and Z-isomers. MS (EI): 316 (M+); 1H NMR (CDCl3) δ 2.13 (s, 18/5 H), 2.24 (s, 12/5 H), 2.40-3.80 (m, 4 H), 6.54 (d, J=5.6 Hz, 2/5 H), 6.53-6.55 (m, 7/5 H), 6.74 (s, 3/5 H), 6.83-6.84 (m, 2/5 H), 6.86 (s, 3/5 H), 6.93 (s, 3/5 H), 7.01-7.02 (m, 1 H), 7.08 (app d, J=5.6 Hz, 2/5 H), 7.14 (app d, J=5.6 Hz, 2/5 H), 7.19-7.25 (m, 4 H), 7.30 (d, J=8.0 Hz, 3/5 H), 7.37-7.39 (m, 2/5 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07411072B2
출처 데이터셋uspto-grants-2008_08
ORD IDord-d4c761dd419b49ebb1e50581ec37c4a2
출처 메모uspto-grants-2008_08