HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(Methylsulfonyl)-3-(trifluoromethyl)phenylhydrazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 4-(Methylsulfonyl)-3-(trifluoromethyl)aniline | HCID 22316682 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Methylsulfonyl)-3-(trifluoromethyl)phenylhydrazine hydrochloride | HCID 22316844 | 79.1% |
Reaction Steps
To a stirred suspension of 4-(methylsulfonyl)-3-(trifluoromethyl)aniline (1.04 g, 4.35 mmol) in conc. HCl (10 mL) was added dropwise a solution of sodium nitrate (0.315 g, 4.57 mmol) in water (10 mL) at −20° C. After stirring for 30 minutes, the resulting suspension was added Tin(II) chloride dihydrate (4.92 g, 21.8 mmol) in conc.HCl (10 mL) at −10° C. After stirring for 1 hour at −5° C., the mixture was stirred further 1 hour at room temperature. The reaction mixture was made alkaline with aqueous NaOH at 0-5° C. The mixture was filtered through Celite, the filterate was extracted with THF (30 mL×3), the combined organic layer washed with brine, dried over MgSO4 and concentration in vacuo to give the subtitle compound (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608095B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-23e4c839f8464fa982d5ea68141f549f |
| Source note | uspto-grants-2003_08 |