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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638755Generated: November 1, 2026

2-Methylbenzenesulfonic acid → 8-[3-Bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylphenyl]-8-azabicyclo[4.3.0]-nonan-7,9-dione

https://huagongshe.com/reaction/1638755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acidHCID 6925—
ReactantHexahydrophthalic anhydride, cis-HCID 641660—
Reactant3-Bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylanilineHCID 19841457—
SolventTolueneHCID 1140—
Product8-[3-Bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylphenyl]-8-azabicyclo[4.3.0]-nonan-7,9-dioneHCID 1984146884.5%

Reaction Steps

To a solution of 3-bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylaniline (4.7 grams, 12.65 mmol) prepared in Part C in toluene (40 milliliters) was added cis-1,2-cyclohexane dicarboxylic anhydride (20.48 grams, 132.83 mmol) and a spatula tipful of toluene sulfonic acid. The reaction mixture was heated at reflux overnight and allowed to cool; washed with 5% NaOH solution (5x), water (3x) and brine (1x); dried over Na2SO4 and concentrated under reduced pressure to afford the crude desired product as a thick brown oil (5.43 grams, 10.69 mmol, 84%) which crystallized on standing and had a melting point of 187° C.-190° C. H'-NMR (CDCl3) 8.40 (d, J=2 Hz, 1H), 8.02 (d,d; J=2, 9 Hz, 1H), 7.00 (br, 5, 1H), 6.55 (d, J=9 Hz, 1H), 3.10 (M, 2H), 2.21 (brS, 6H), 1.93 (M, 4H), 1.58 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880838
Source datasetuspto-grants-1989_11
ORD IDord-cceddabcfc5d4b9f8fc2afccc6f454c5
Source noteuspto-grants-1989_11