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HRID 231404作成日:2026年10月27日

Benzyl Bromide → Benzyl 2-formylbenzoate

https://huagongshe.com/reaction/231404

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Phthalaldehydic acidHCID 8406—
反応物Potassium CarbonateHCID 11430—
溶媒AcetoneHCID 180—
生成物Benzyl 2-formylbenzoateHCID 24609684.9%

反応手順

A mixture of 2-carboxybenzaldehyde (15.00 g, 0.100 moles), benzyl bromide (20.52 g, 0.120 moles) and potassium carbonate (41.46 g, 0.300 moles) in 250 ml of acetone under nitrogen in a 500 ml round-bottom flask equipped with a magnetic stirrer was refluxed for 6 hours and then stirred at room temperature overnight. The mixture was then filtered through Celite and the filtrate concentrated in vacuo to remove the acetone. The remaining yellow oil was dissolved in ether (200 ml) and this solution washed with saturated sodium bicarbonate solution (1×50 ml), saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo to give 20.4 g of the product as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04846873
出典データセットuspto-grants-1989_07
ORD IDord-a445ef4974ce4d15b7c1f5befa2f0893
出典メモuspto-grants-1989_07