Pyridine → HCID 90349596, compound

Under a nitrogen atmosphere, 4-iodobenzoic acid (1a) (10.6 g, 42.9 mmol) was dissolved in anhydrous dichloromethane (140 mL), and several drops of anhydrous N,N-dimethylformamide were added. Thereafter, oxalyl chloride (4.50 mL, 42.4 mmol) was added at 0° C., and the mixture was stirred at room temperature for 10 hr. The solvent was removed, anhydrous pyridine (70 mL) and n-heptanol (7.0 mL, 49.4 mmol) were added, and the mixture was stirred at 70° C. for 5 hr. The reaction solvent was removed, the residue was diluted with ethyl acetate, washed with distilled water and saturated aqueous sodium hydrogen carbonate solution, and the organic layer was dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (ethyl acetate:hexane=1:19) to give heptyl 4-iodobenzoate (2a) (14.5 g, yield 97%) as an oily liquid.

1. customThe solvent was removed
2. stirringthe mixture was stirred at 70° C. for 5 hr
3. customThe reaction solvent was removed
4. additionthe residue was diluted with ethyl acetate
5. washwashed with distilled water and saturated aqueous sodium hydrogen carbonate solution
6. dry with materialthe organic layer was dried over anhydrous sodium sulfate
7. customThe solvent was removed under reduced pressure
8. customthe residue was purified by column chromatography (ethyl acetate:hexane=1:19)

ORD record

ord-f00140c0cfda4099b6ba90d17f7ab767

Source dataset

uspto-grants-2016_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09290592B2