HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392440Generated: October 26, 2026
Ethanol → (5-Amino-2-chlorophenyl)(phenyl)methanone
https://huagongshe.com/reaction/392440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 2-Chloro-5-nitrobenzophenone | HCID 118591 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (5-Amino-2-chlorophenyl)(phenyl)methanone | HCID 10489713 | — |
Reaction Steps
2-Chloro-5-nitrobenzophenone (1.3 g,5.0 mmol), tin(II) chloride (4.5 g, 20 mmol), and ethanol (20 ml) were mixed and heated at 70° C. for 1 h. After cooling to room temperature, to the reaction mixture were added ice, EtOAc and aqueous NaHCO3 and it was stirred for 30 min. The organic layer was washed with brine and dried over MgSO4. Filtration and evaporation afforded 5-amino-2-Chlorobenzophenone. 1H NMR, 7.85(m,2H), 7.30-7.66 (m,3H7.20 (d,1H,J=8.8 Hz), 6.60-6.80 (m,2H). MS calcd 231.1; MS (M+1) 232.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800651B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-e1b29d11510c40008c7c6efbe6135613 |
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| Source note | uspto-grants-2004_10 |
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