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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2168311생성일: 2026년 10월 25일

Formaldehyde → 6-bromo-2-methylene-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/2168311

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Trifluoroacetic acidHCID 6422—
반응물Phenylboronic AcidHCID 66827—
반응물1-Indanone, 6-bromo-HCID 139778—
용매TolueneHCID 1140—
생성물6-bromo-2-methylene-2,3-dihydro-1H-inden-1-oneHCID 5819716630%

반응 단계

A solution of 6-bromo-2,3-dihydro-1H-inden-1-one (0.3 g, 1.36 mmol), paraformaldehyde (0.4 g, 13.6 mmol), phenylboronic acid (0.2 g, 1.64 mmol) and trifluoroacetic acid (0.1 mL, 0.15 g, 1.36 mmol) in dry toluene (10 mL) was refluxed for 5 hours. When starting material was totally consumed, the crude mixture was cooled to room temperature, neutralized with saturated aqueous Na2CO3, extracted with ethyl acetate, dried and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, petroleum ether-ethyl acetate, 95:5) to give compound 6-bromo-2-methylene-2,3-dihydro-1H-inden-1-one (89 mg, 30%) as a white solid. 1H NMR (CDCl3, 400 MHz): 3.71 (s, 2H), 5.68 (s, 1H), 6.39 (s, 1H), 7.38-7.40 (d, 1H), 7.70-7.72 (d, 1H), 7.99 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09045500B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-4263e9ef95164dd0930c99abca3b5606
출처 메모uspto-grants-2015_06