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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336564생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/336564

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 번호US08889703B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-0f9d7639db5549acbced89851d0d158f
출처 메모uspto-grants-2014_11