HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoyl chloride → 2-(4-Nitrophenyl)Benzo[D]Thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(4-Nitrophenyl)Benzo[D]Thiazole | HCID 827500 | 73.2% |
Reaction Steps
A solution of 4-nitrobenzoyl chloride (1.49 g, 8.0 mmol) in benzene anhydrous, 10 mL) was added dropwise to 2-aminothiophenol (1.0 g, 8.0 mmol in 10 ml of benzene) at room temperature. The reaction mixture was allowed to stir for 16 hr. The reaction was quenched with water (20 mL). The aqueous layer was separated and extracted with ethyl acetate (3×10 ml). The combined organic layers were dried and evaporated. The crude product was purified with flush column, (hexane:ethyl acetate=85:15) to give 1.5 g (73.2%) of product as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351401B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-5604215748e24f859d16b9a30f4d0eab |
| Source note | uspto-grants-2008_04 |