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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | Hexahydrophthalic anhydride, cis- | HCID 641660 | — |
| Reactant | 3-Bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylaniline | HCID 19841457 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 8-[3-Bromo-4-(2-chloro-4-nitrophenoxy)-2,5-dimethylphenyl]-8-azabicyclo[4.3.0]-nonan-7,9-dione | HCID 19841468 | 84.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04880838 |
|---|
| Source dataset | uspto-grants-1989_11 |
|---|
| ORD ID | ord-cceddabcfc5d4b9f8fc2afccc6f454c5 |
|---|
| Source note | uspto-grants-1989_11 |
|---|