Hydrochloric Acid → 1-{5-Bromo-2-[(3-chloropropyl)sulfanyl]phenyl}hydrazine
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][CH2:10][CH2:11][CH2:12][Cl:13])=[C:6]([CH:8]=1)[NH2:7].Cl.[N:15]([O-])=O.[Na+].O.O.Cl[Sn]Cl>C(O)(C(F)(F)F)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][CH2:10][CH2:11][CH2:12][Cl:13])=[C:6]([NH:7][NH2:15])[CH:8]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
5-Bromo-2-[(3-chloropropyl)sulfanyl]aniline (0.938 g, 3.3 mmol) was dissolved in TFA (4 mL). The reaction flask was cooled to 0° C. and HCl (15 mL) was added. To the resulting suspension, an aqueous solution of NaNO2 (0.25 g, 3.7 mmol, 3 mL H2O) was slowly added. The flask was warmed to rt and stirred for 2 hrs. The flask was re-cooled to 0° C. and was transferred via cannula to an aqueous solution of SnCl2.2H2O (1.49 g, 6.6 mmol, 3 mL of H2O). The solution was stirred for 3 hours. The precipitate was collected by filtration and the residue was air-dired overnight. 1-{5-bromo-2-[(3-chloropropyl)sulfanyl]phenyl}hydrazine hydrochloroide was isolated (0.800 g, 73%) was a light-brown powder. 1H NMR (CD3OD, 300 Mhz) δ7.42 (d, 1H, 8.0 Hz), 7.14-7.21 (m, 2H), 3.66 (t, 2H, 6.2 Hz), 2.97 (t, 2H, 6.9 Hz), 1.90-1.99 (m, 2H) ppm. MS (CI, NH3): 297 (base, M+H).
Workup
- temperatureThe flask was warmed to rt
- temperatureThe flask was re-cooled to 0° C.
- stirringThe solution was stirred for 3 hours
- filtrationThe precipitate was collected by filtration
- waitthe residue was air-dired overnight
Sources & evidence
- ORD record
- ord-126be1b41bbd4d29bec0881b835db292
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06713471B1
Reaction notes
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