HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1,3-Dibenzyl 5-nitrobenzene-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Nitroisophthalic acid | HCID 12069 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Dibenzyl 5-nitrobenzene-1,3-dicarboxylate | HCID 19063926 | 76.7% |
Reaction Steps
In DMF (60 mL) was stirred 5-nitro-1,3-benzenedicarboxylic acid (2.1 g, 10 mmol) and potassium carbonate (8.3 g, 60 mmol). To this was added benzyl bromide (3.60 g, 21 mmol) and the mixture stirred at room temperature for 18 hours. The mixture was then filtered free of solids and the DMF solution evaporated at reduced pressure to give an oil. The oil was partitioned between methylene chloride (100 mL) and 10% citric acid solution (100 mL). The organic phase was separated, washed successively with saturated sodium bicarbonate solution (100 mL) and then brine (100 mL). The organic phase was dried over magnesium sulfate and evaporated at reduced pressure to give 1.5 g (39%) of the solid diester. MS: M-benzyl=300.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214712B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-59228f2f3df94d35acdd9a5969d726f3 |
| Source note | uspto-grants-2007_05 |