Ethylene Glycol → HCID 14008100, compound

HRID 1927692Notes

Reaction equation

Br[C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:23])[N:7]([C:16]3[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=3)[C:8](=[O:15])[C:9]3[C:14]=2[C:13]=1[CH:12]=[CH:11][CH:10]=3.[OH-].[Na+].[CH2:26]([OH:29])[CH2:27][OH:28]>O>[OH:28][CH2:27][CH2:26][O:29][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:23])[N:7]([C:16]3[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=3)[C:8](=[O:15])[C:9]3[C:14]=2[C:13]=1[CH:12]=[CH:11][CH:10]=3

Participants

Conditions

Temperature: 120 °C

Procedure

A mixture of 6-bromo-2-p-tolyl-benzo[de]isoquinoline-1,3-dione (4.0 g), sodium hydroxide (0.65 g), and 1,2-ethylene glycol (50 ml) was maintained under reflux with stirring at 120° C. for 10 hrs. The reaction mixture was then cooled to room temperature and water (100 ml) was added to the mixture. The solid that separated out was filtered, washed with water, and dried at 100° C. for 8 hours (Yield=2.71 g). The crude product was purified using 120 ml monochlorobenzene and 0.25 g activated charcoal to obtain pure product weighing 1.32 g. H1-NMR: 2.39 δ (s, 3 protons); 3.92 δ (m, 2 proton); 4.35 δ (t, 2 protons); 5.13 δ (t, 1 proton); 7.22 δ (m, 2 protons); 7.31 δ (m, 3 protons); 7.83 δ (t, 1 proton); 8.44 δ (m, 2 protons); 8.68 δ (d, 1 proton).

Workup

temperaturewas maintained
temperatureunder reflux
temperatureThe reaction mixture was then cooled to room temperature
customThe solid that separated out
filtrationwas filtered
washwashed with water
customdried at 100° C. for 8 hours (Yield=2.71 g)
customThe crude product was purified
customto obtain pure product

Sources & evidence

ORD record: ord-65ccd2d78d054f14a6a5ad609071a9e5
Source dataset: uspto-grants-2012_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08183310B2

Reaction notes

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