Diethyl Ether → HCID 10751866、化合物

A solution of 2-bromo-4-methylphenol methoxymethyl ether (9.49 g) in diethyl ether (170 ml) was cooled to -78° C. To the solution was added dropwise a 1.6M solution of n-butyl lithium hexane solution (30 ml) under argon atmosphere. The mixture was stirred for 45 minutes, to which was then added dropwise 2-cyano-3-trimethylsilyloxy pyridine (8.13 g) at -78° C. Then, the cooling bath was removed, and the mixture was stirred for 3 hours while warming up to room temperature. To the reaction mixture was added methanol (10 ml) to quench the reaction, then the solvent was distilled off under reduced pressure. To the residue were added methanol (100 ml), THF (25 ml) and 2N HCl (60 ml). The mixture was stirred overnight at room temperature, which was then heated for 2 hours under reflux. The reaction mixture was cooled by aeration, which was neutralized with an aqueous solution of sodium hydroxide, which was concentrated, followed by extraction with ethyl acetate. The extract was dried (anhydrous magnesium sulfate), then the solvent was distilled off, and the residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 2-(2-hydroxy-5-methylbenzoyl)-3-hydroxypyridine (7.72 g) (Compound A-4), whose physical properties and spectrum data are shown in Table 1 and Table 3.

1. customThen, the cooling bath was removed
2. stirringthe mixture was stirred for 3 hours
3. additionTo the reaction mixture was added methanol (10 ml)
4. customto quench
5. customthe reaction
6. distillationthe solvent was distilled off under reduced pressure
7. additionTo the residue were added methanol (100 ml), THF (25 ml) and 2N HCl (60 ml)
8. stirringThe mixture was stirred overnight at room temperature
9. temperaturewhich was then heated for 2 hours
10. temperatureunder reflux
11. temperatureThe reaction mixture was cooled by aeration, which
12. concentrationwas concentrated
13. extractionfollowed by extraction with ethyl acetate
14. dry with materialThe extract was dried (anhydrous magnesium sulfate)
15. distillationthe solvent was distilled off
16. customthe residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane)

ORDレコード

ord-97c389b9efb04eddb8562070dea9bece

出典データセット

uspto-grants-1998_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05716971