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HRID 59181作成日:2026年10月26日

Benzyl Chloride → Dibenzyl 2,3-bis(benzyloxy)terephthalate

https://huagongshe.com/reaction/59181

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物Potassium CarbonateHCID 11430—
反応物2,3-Dihydroxyterephthalic acidHCID 88273—
溶媒DimethylformamideHCID 6228—
生成物Dibenzyl 2,3-bis(benzyloxy)terephthalateHCID 11813603348%

反応条件

温度67 °C

反応手順

1 (101.798 g, 0.514 mol), benzyl chloride (258 mL, 2.242 mol), KI (25.304 g, 0.140 mol), K2CO3 (664.270 g, 4.806 mol), and 1.3 L DMF were combined in a 5-L 3-neck round-bottom flask, yielding a mixture of dark brown solution and undissolved solid. The flask was fitted with a reflux condenser and mechanical stirrer, and placed in a heating mantle. The reaction mixture was heated at 67° C. for 3 d and filtered. The dark brown, clear filtrate was rotovapped to ˜400 mL of opaque, brown, viscous oil, which was dissolved in ˜600 mL DCM. The opaque, brown solution was filtered and extracted with water (5×500 mL). A small amount of brine was used to break up emulsions. The organic layer was dried with MgSO4 and rotovapped to ˜250 mL of dark brown oil. This oil was purified by silica column chromatography (0-5% MeOH in DCM) to yield a hardened brown oil (48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09439984B2
出典データセットuspto-grants-2016_09
ORD IDord-eeb610df79ef4d38baac448a9bd8ddae
出典メモuspto-grants-2016_09