Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (2,4-Dimethylphenyl)boronic acid | HCID 4198739 | — |
| Product | HCID 21877560 | HCID 21877560 | 47% |
Reaction Steps
To fuming nitric acid (1 ml) cooled to −40° C. was added TFA (1 ml). The resulting mixture was allowed to warm slightly to −35° C. and 2,4-dimethyl phenyl boronic acid (150 mg, 1 mmol) was added in one portion. After 1 h, ice was added and the heterogenous mixture was filtered. The resulting solid was suspended in Et2O and extracted with 3N NaOH (aq) (1 ml) then water (2 ml). The aqueous phase was acidified with 3N HCl (aq) (1 ml) and back extracted with EtOAc (3×5 ml). The pooled organics were washed with brine, dried with Na2SO4 decanted and concentrated to give 2,4-dimethyl-5-nitro-phenyl boronic acid (93 mg, 47%). LCMS (ESI+) [M+H]/z Calc'd 196. found 196.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141587B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-a34296e8e7e546ddaf785231156dcdae |
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| Source note | uspto-grants-2006_11 |
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