HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-nitrobenzene → Methyl 5-chloro-2-nitrobenzeneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Tris(dimethylamino)sulfonium difluorotrimethylsilicate | HCID 9795567 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-chloro-2-nitrobenzeneacetate | HCID 13265167 | — |
Reaction Steps
To a solution of 1.576 g (10 mmol) of 4-chloronitrobenzene and 1.68 mL (10.22 mmol) of carbomethyoxymethyltrimethylsilane in anhydrous THF was added 2.751 g (10 mmol) of TASF in 5 mL of acetonitrile at -78° C. The mixture was stirred for 7 hrs at that temperature, and 0.50 mL (9.70 mmol) of bromine was added dropwise. Stirring was continued for 1 hr, and saturated sodium bisulfite was added. The product was extracted into ether and isolated by chromatography on silica using 30% ether/hexane as solvent. The yield was 1.15 g (50%) product, which was an oil. The product was analyzed by infrared spectroscopy and nuclear magnetic resonance spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05164499 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-aa1de066d33b43b8aba44f19f860e89f |
| Source note | uspto-grants-1992_11 |