Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-{3-[3-(Trifluoromethyl)-3H-diaziren-3-yl]phenyl}formamide | HCID 14896211 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14896212 | HCID 14896212 | — |
Reaction Steps
N-formyl m-[3-(trifluoromethyl)diazirine-3-yl]aniline (120 mg) is dissolved in 3 ml of methanol. Concentrated HCl (1 ml) is added. The mixture is reacted for 10 min at ambient temperature. The reaction mixture is cooled to 0° C. in an ice bath and neutralised with NaOH (3 ml, 6N). The aqueous phase is extracted with ethyl ether (5 times 4 ml). The combined organic phase is washed with deionised water (5 ml) and dried over MgSO4. The solvent is evaporated under reduced pressure to give a yellow oil m-[3-(trifluoromethyl)-diazirine-3-yl]aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06780980B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-cfe358ec772c4cf3a31c5696604a367a |
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| Source note | uspto-grants-2004_08 |
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