HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 4-(2-Amino-4-thiazolyl)-2-methoxy-6-nitrophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone | HCID 14450983 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Amino-4-thiazolyl)-2-methoxy-6-nitrophenol | HCID 21459203 | — |
Reaction Steps
aaa) A suspension of 2.9 g of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone and 761.2 mg of thiourea in 170 ml of ethanol is treated at 60° with 820.3 mg of sodium acetate and stirred for 6 hours. The reaction mixture is then evaporated, the residue is treated with 170 ml of water and heated to 60° for 30 minutes. After cooling the product is filtered under suction and washed with water. There is obtained 4-(2-amino-4-thiazolyl)-2-methoxy-6-nitrophenol of m.p. 248°-250° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389653 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-c3e529e313334920b3472eced7f1ee5b |
| Source note | uspto-grants-1995_02 |