反应 #1151

反应方程式

ethyl acetate

Boron tribromide

methyl 6-methoxybenzofuran-2-carboxylate

→

methyl 6-hydroxybenzofuran-2-carboxylate

收率 73.0%

溶剂

dichloromethane

反应条件

后处理

1. 1
   洗涤After the organic layer was washed with water
2. 2
   干燥dried (MgSO4)
3. 3
   workup.DISTILLATIONthe solvent was distilled off
4. 4
   workup.ADDITION10% hydrochloric acid-methanol (60 ml) was added to the residue
5. 5
   温度by heating at 70° to 80° C. for 5 hours
6. 6
   浓缩The reaction mixture was concentrated under reduced pressure
7. 7
   过滤the resulting crystals of methyl 6-hydroxybenzofuran-2-carboxylate (10.75 g) were collected by filtration
8. 8
   浓缩The filtrate was concentrated
9. 9
   洗涤From the fraction eluted with diethyl ether-hexane (1:2

实验过程

Boron tribromide (24.9 g) was added dropwise to a solution of methyl 6-methoxybenzofuran-2-carboxylate (18.6 g) in dichloromethane (200 ml) at 0° C., followed by stirring at room temperature for 1 day. The reaction mixture was poured over ice water; ethyl acetate (300 ml) was added. After the organic layer was washed with water and dried (MgSO4), the solvent was distilled off; 10% hydrochloric acid-methanol (60 ml) was added to the residue, followed by heating at 70° to 80° C. for 5 hours. The reaction mixture was concentrated under reduced pressure; the resulting crystals of methyl 6-hydroxybenzofuran-2-carboxylate (10.75 g) were collected by filtration using diethyl ether-isopropyl ether (2:1, v/v). The filtrate was concentrated; the residue was subjected to silica gel column chromatography. From the fraction eluted with diethyl ether-hexane (1:2, v/v), methyl 6-hydroxybenzofuran-2-carboxylate (1.75 g) was obtained (total yield 73%), which was then recrystallized from diethyl ether-isopropyl ether to yield colorless prisms having a melting point of 176° to 177° C.

来源