Water → HCID 10445976, compound

HRID 1463425Notes

Reaction equation

C([Li])CCC.Br[C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1.[CH3:13][C:14]1[C:21]([O:22][CH3:23])=[C:20]([CH3:24])[CH:19]=[C:18]([O:25][CH3:26])[C:15]=1[CH:16]=[O:17].O>CCCCCC.CCOCC.O1CCCC1>[N:9]1[CH:10]=[CH:11][CH:12]=[C:7]([CH:16]([OH:17])[C:15]2[C:14]([CH3:13])=[C:21]([O:22][CH3:23])[C:20]([CH3:24])=[CH:19][C:18]=2[O:25][CH3:26])[CH:8]=1

Participants

Conditions

Temperature: -60 °C

Procedure

Then 48 ml of a 1.6M solution of n-butyllithium in hexane was added thereto. After cooling to -60° C., 7.4 ml of 3-bromopyridine was added thereto in portions. Then the mixture was stirred at -60° C. for 30 minutes and a solution of 9.9 g of 2,4-dimethyl-3,6-dimethoxybenzaldehyde in 100 ml of dry ether and 40 ml of dry tetrahydrofuran was added dropwise thereto. After the completion of the addition, the cooling bath was taken off. When the temperature of the reaction mixture reached -10° C., water was added thereto and the mixture was extracted with ethyl acetate. After washing with a saline solution and drying, the solvent was distilled off. Then the residue was purified by silica gel column chromatography (ethyl acetate: hexane=1:5-5:1). Thus 14.0 g of the title compound was obtained.

Workup

additionAfter the completion of the addition
customreached -10° C.
extractionthe mixture was extracted with ethyl acetate
washAfter washing with a saline solution
customdrying
distillationthe solvent was distilled off
customThen the residue was purified by silica gel column chromatography (ethyl acetate: hexane=1:5-5:1)

Sources & evidence

ORD record: ord-fc834ceda9dc426a868cbf84c5eee141
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05300518

Reaction notes

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