Hydrochloric Acid → HCID 59326519, compound

To a mixture of the above prepared (4-acetoxy-6-fluoro-3-methyl-naphthalen-2-yl)-acetic acid tert-butyl ester (28.4 g, 85.44 mmol) in 140 mL of methanol was added sodium methoxide (25% solution in methanol, 23.44 mL, 102.5 mmol) rapidly dropwise. The resulting reaction mixture was stirred at room temperature for 20 minutes, when HPLC analysis indicated a completed reaction. The mixture was cooled to 0° C., and then acidified to pH 2 with 1N hydrochloric acid solution (111.1 mL, 111.1 mmol). The mixture was then stirred at 0-5° C. for an additional 30 minutes. The resulting solid was filtered, and washed with water (2×40 mL), then dried under vacuum overnight (40° C.), to produce 23.7 g of a light yellow solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 9.09 (s, 1H), 7.76-7.86 (m, 2H), 7.26-7.35 (m, 2H), 3.71 (s, 2H), 2.23 (s, 3H), 1.41 (s, 9H).

1. additionTo a mixture of the
2. customThe resulting reaction mixture
3. customa completed reaction
4. temperatureThe mixture was cooled to 0° C.
5. stirringThe mixture was then stirred at 0-5° C. for an additional 30 minutes
6. filtrationThe resulting solid was filtered
7. washwashed with water (2×40 mL)
8. customdried under vacuum overnight (40° C.)

ORD record

ord-1ed7d716130440a3a171b4f53edc22cf

Source dataset

uspto-grants-2014_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08642629B2