2,5-Dichloronitrobenzene → HCID 19377564, compound

HRID 1464440Notes

Reaction equation

[Cl:1][C:2]1[CH:9]=[C:6]([CH:7]=[O:8])[C:5]([OH:10])=[CH:4][CH:3]=1.[H-].[Na+].Cl[C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=1[N+:21]([O-:23])=[O:22]>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=2[N+:21]([O-:23])=[O:22])=[C:6]([CH:9]=1)[CH:7]=[O:8]

Participants

Conditions

Temperature: 100 °C

Procedure

To a stirred solution of 5-chlorosalicylaldehyde (8.56 g) in N,N-dimethylformamide (90 mL) under nitrogen was added, in portions, sodium hydride (1.37 g). To the resulting solution was added 2,5-dichloro-1-nitrobenzene (10.0 g) and N,N-dimethylformamide (10 mL), and the reaction was heated at 100° C. under nitrogen for 6 hours. The reaction was evaporated under vacuum, and the residue was partitioned between chloroform and 1 N NaOH. The layers were separated, and the aqueous layer was extracted once more with chloroform. The combined chloroform extracts were washed with 1 N NaOH, water, 1 N HCl, water, and brine, dried over magnesium sulfate, and evaporated under vacuum. Crystallization from methanol yielded the title compound as a yellow solid. Mp: 128°-130° C.

Workup

customThe reaction was evaporated under vacuum
customthe residue was partitioned between chloroform and 1 N NaOH
customThe layers were separated
extractionthe aqueous layer was extracted once more with chloroform
washThe combined chloroform extracts were washed with 1 N NaOH, water, 1 N HCl, water, and brine
dry with materialdried over magnesium sulfate
customevaporated under vacuum
customCrystallization from methanol

Sources & evidence

ORD record: ord-a6b75b62daca45edb00134ff94c125a7
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05304644

Reaction notes

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