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HRID 2168311作成日:2026年10月27日

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

https://huagongshe.com/reaction/2168311

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Trifluoroacetic acidHCID 6422—
反応物Phenylboronic AcidHCID 66827—
反応物1-Indanone, 6-bromo-HCID 139778—
溶媒TolueneHCID 1140—
生成物6-bromo-2-methylene-2,3-dihydro-1H-inden-1-oneHCID 5819716630%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09045500B2
出典データセットuspto-grants-2015_06
ORD IDord-4263e9ef95164dd0930c99abca3b5606
出典メモuspto-grants-2015_06