HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 4-(4-Nitrobenzyl)-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 4-Benzylbenzoic acid | HCID 136429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Nitrobenzyl)-benzoic acid | HCID 21876878 | 58% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
70% Nitric acid (3.16 mL) was added dropwise to a suspension of trifluoromethanesulfonic acid (9.34 mL, 105.6 mmol) in dichloromethane (250 mL). The suspension was cooled in a dry ice-acetone bath and a solution of 4-benzyl-benzoic acid (10.19 g, 48 mmol) in dichloromethane (50 mL) was added dropwise. The mixture was stirred for about 2 hours at −78° C. and an additional 2 hours at room temperature. The reaction mixture was poured into crushed Ice. The separated organic layer was washed with dichloromethane (2×) and the combined organic layers were dried over (Na2SO4), and solvents were evaporated. Recrystallization of the crude product from methanovethyl acetate gave 4-(4-nitrobenzyl)-benzoic acid (9.27 g, 58%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06693200B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-68f6cfd82dd743b0a0b33e43e520cf29 |
| Source note | uspto-grants-2004_02 |