HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183098Generated: November 1, 2026
Stannous Chloride → 5-Methyl-3-phenyl-1H-indazole
https://huagongshe.com/reaction/2183098
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 2-Amino-5-methylbenzophenone | HCID 87335 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Methyl-3-phenyl-1H-indazole | HCID 610412 | 80.4% |
Reaction Steps
To a solution of 2-amino-5-methylphenyl phenyl ketone (2.0 g, 9.5 mmol) in HCl (45 mL of a 6M solution) at 0° C. was added sodium nitrite (NaNO2) (719 mg, 10.4 mmol) in water (2 mL). The reaction was stirred for 30 min when the homogeneous solution was added dropwise to a solution of SnCl2 (5.88, 26 mmol) in concentrated HCl (15 mL) at room temperature. The reaction was stirred for 30 min when it was filtered. The solid was then taken up in ethyl acetate (80 mL) and saturated sodium bicarbonate (80 mL). The suspension was then filtered and the ethyl acetate layer dried (Na2SO4) and concentrated to give the product (1.59 g, 80% yield). (1H NMR (DMSO-d6) δ 7.96 (d, 2H), 7.85 (br s, 1H), 7.54-7.46 (m, 3H), 7.39 (t, 1H), 7.24 (d, 1H), 2.45 (s, 3H); ES-MS (m/z) 209 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897231B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-928f0a7d5ff54bdc82b98b42e63f5539 |
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| Source note | uspto-grants-2005_05 |
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