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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2168311Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2168311

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
PatentnummerUS09045500B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-4263e9ef95164dd0930c99abca3b5606
Quellennotizuspto-grants-2015_06