Hydrochloric Acid → HCID 54043883, compound

A solution of 3-bromo-5-fluoroethoxynitrobenzene, as described above in Step D, (990 mg, 3.75 mmol) in tetrahydrofuran (22 mL) was added to a mixture of NaBH4/S3 (1.2 g) in tetrahydrofuran (15 mL) and the resulting mixture was placed in a 60° C. oil bath and heated overnight. The reaction was cooled to room temperature and concentrated using the rotary evaporator giving a yellow solid. Diethyl ether was added and 10% HCl until the pH was 1. The resulting mixture was filtered through celite and the layers were separated. The aqueous layer was washed with diethyl ether. The aqueous layer was made basic (pH>10) with diethyl ether present, the layers were separated and the aqueous layer was extracted with diethyl ether and ethyl acetate. The organic layers were combined and dried (MgSO4), filtered and concentrated in vacuo to give 3-bromo-5-fluoroethoxyaniline as a yellow oil.

1. customwas placed in a 60° C.
2. temperatureheated overnight
3. concentrationconcentrated
4. customthe rotary evaporator
5. customgiving a yellow solid
6. filtrationThe resulting mixture was filtered through celite
7. customthe layers were separated
8. washThe aqueous layer was washed with diethyl ether
9. customthe layers were separated
10. extractionthe aqueous layer was extracted with diethyl ether and ethyl acetate
11. dry with materialdried (MgSO4)
12. filtrationfiltered
13. concentrationconcentrated in vacuo

ORD record

ord-039d0b84bf4245ea98b82b9a3ade0091

Source dataset

uspto-grants-2002_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06458935B1