HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538146Generated: October 31, 2026
Dimethylformamide → HCID 66937462, compound
https://huagongshe.com/reaction/538146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,5-Dichloro-2-nitroaniline | HCID 81149 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66937462 | HCID 66937462 | 56% |
Reaction Steps
To a mixture of 4,5-dichloro-2-nitro-phenylamine (3.00 g, 14.5 mmol) and DMF (72 mL) was added K2CO3 (5.31 g, 29.0 mmol) and phenyl-methanethiol (3.94 g, 31.7 mmol). The mixture was heated to 70° C. for 18 h and then cooled to 23° C. The reaction mixture was dissolved in EtOAc (200 mL), washed with saturated sodium bicarbonate solution (100 mL), washed with brine (3×100 mL). The organic layers were combined, dried, filtered, and concentrated under reduced pressure. The residue was purified (FCC) (5-45% EtOAc/hexanes) to yield the titled compound (2.39 g, 56%). MS (ESI/CI): mass calcd. for C13H11ClN2O2S, 294.0; m/z found, 295.0 [M+H]+. 1H NMR (600 MHz, DMSO-d6): 7.96 (s, 1H), 7.56 (s, 2H), 7.50 (d, J=7.2 Hz, 2H), 7.37 (t, J=7.5 Hz, 2H), 7.31 (t, J=7.4 Hz, 1H), 7.05 (s, 1H), 4.27 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865713B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-d6644c54aa204ceda6f6572336092e67 |
|---|
| Source note | uspto-grants-2014_10 |
|---|