HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous chloride dihydrate → 2-(4-Aminophenyl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 2-(4-Nitrophenyl)Benzo[D]Thiazole | HCID 827500 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Aminophenyl)benzothiazole | HCID 234475 | — |
Reaction Steps
A mixture of 2-(4-nitrophenyl)benzothiazole (105 mg, 0.40 mmol) and tin (II) chloride dihydrate (205 mg, 0.91 mmol) in ethanol (20 mL) was refluxed under N2 for 4 hrs. After removing ethanol by vacuum evaporation. The residue was dissolved into ethyl acetate (20 ml), and washed with NaOH solution (1 N, 3×20 ml) and water (3×20 ml), dried and evaporated to dryness to givelo2 mg (97%) of the product
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351401B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-5c2f6336a6d34209a0779a29b4d4dd21 |
| Source note | uspto-grants-2008_04 |