Methanol → 6-Hydroxy-1,3-dihydro-2-benzofuran-1-one

A solution of 6-methoxy-3H-isobenzofuran-1-one (50 g, 0.3 moles), prepared as described in example 34, in CH2Cl2 (250 ml) under N2 at −5° C., was dropwise added with BBr3 (360 ml 0.36 moles). At the end of the addition the solution was stirred at room temperature overnight, then cooled and added with further BBr3 (60 ml, 60 mmoles). The stirring was kept on for 4 hours at room temperature. The mixture was cooled and added with CH3OH (250 ml), then dried under vacuum to give a solid which was triturated in ethyl ether and washed with ethyl ether and ethyl acetate. After drying under vacuum at 40° C. a solid was obtained which was joined to the solid yielded by drying the mother liquors, discolouring and triturating in ethyl ether. There were obtained 33.51 g of the title compound (yield: 73%).

1. additionAt the end of the addition the solution
2. temperaturecooled
3. customwas kept on for 4 hours at room temperature
4. temperatureThe mixture was cooled
5. customdried under vacuum
6. customto give a solid which
7. customwas triturated in ethyl ether
8. washwashed with ethyl ether and ethyl acetate
9. customAfter drying under vacuum at 40° C. a solid
10. customwas obtained which
11. customyielded
12. customby drying the mother liquors
13. customtriturating in ethyl ether

ORDレコード

ord-d4f6adb592a84895b93284cb58f674a8

出典データセット

uspto-grants-2001_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06329370B1