Phthalimide → Sodium 2-methylbenzenesulfonate

HRID 2186639Notes

Reaction equation

C[C:2]1[CH:7]=[CH:6][C:5]([S:8]([O-:11])(=[O:10])=[O:9])=[CH:4][C:3]=1C.[Na+:13].[C:14]1(=O)NC(=O)C2=CC=CC=C12>>[C:4]1([CH3:14])[C:5]([S:8]([O-:11])(=[O:9])=[O:10])=[CH:6][CH:7]=[CH:2][CH:3]=1.[Na+:13]

Participants

Reactant 2

HCID 6809Phthalimide

HCID 23668192Sodium Xylenesulfonate

Product 1

HCID 23681382Sodium 2-methylbenzenesulfonate

Procedure

The procedure of Example 2 was repeated using 30.6 grams Naxonate ST, a commercially available sodium toluene sulfonate from Ruetgers-Naese (0.15 mol sodium toluene sulfonate with a content of 93%) instead of phthalimide to yield a product in which toluene sulfonic acid methyl 6,13-dihydro quinacridone having a molecular weight of 500 was detected by MALDI.

Sources & evidence

ORD record: ord-912a4688444548eb8677ed4ad5a2c8dc
Source dataset: uspto-grants-2002_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06406533B2

Reaction notes

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