HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 2-amino-3-chloro-N-(2-chlorophenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Amino-3-chlorobenzoic acid | HCID 80807 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-amino-3-chloro-N-(2-chlorophenyl)benzamide | HCID 22316585 | 78.8% |
Reaction Steps
Prepared according to Procedure A using 2-amino-3-chlorobenzoic acid (1.0 g, 5.82 mmol) and SOCl2 (1.1 mL, 14.6 mmol) in benzene (25 mL), followed by 2-chloroaniline (1.2 mL, 11.7 mmol) and CHCl3 (25 mL). The product was recrystallized from MeOH to provide 1.29 g of a yellow solid (78%). 1H NMR (CDCl3) δ: 8.43 (dd, J=1.4, 8.3 Hz, 1H); 8.30 (br s, 1H); 7.47 (dd, J=1.1, 8.0 Hz, 1H); 7.42 (d, J=8.0 Hz, 2H); 7.33 (dt, J=1.4, 7.9 Hz, 1H); 7.09 (dt, J=1.5, 7.7 Hz, 1H); 6.68 (t, J=7.9 Hz, 1H); 6.13 (br s, 2H). MS (ES): m/z 281.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492389B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-010c4c8b5d534096b5e35040731bc308 |
| Source note | uspto-grants-2013_07 |