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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336564Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/336564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktTrifluoroacetic acidHCID 6422—
EduktPhenylboronic AcidHCID 66827—
Edukt1-Indanone, 6-bromo-HCID 139778—
LösungsmittelTolueneHCID 1140—
Produkt6-bromo-2-methylene-2,3-dihydro-1H-inden-1-oneHCID 5819716630%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889703B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-0f9d7639db5549acbced89851d0d158f
Quellennotizuspto-grants-2014_11