HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(2-bromoethyl)thiophene → HCID 21520086, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(2-bromoethyl)thiophene | HCID 10877948 | — |
| Reactant | 5-Amino-3-mercapto-4-phenoxybenzoic acid | HCID 21520107 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21520086 | HCID 21520086 | — |
Reaction Steps
To a solution of 5-amino-3-mercapto-4-phenoxybenzoic acid (2.5 g) in 0.5 N sodium hydroxide (100 ml), a solution of 3-bromoethylthiophene (3.5 g in benzene (20 ml)) is added. The reacton mixture is stirred for 2 hours at room temperature. After extraction with additional benzene, the aqueous layer is acidified by addition of 4 N hydrochloric acid to precipitate 5-amino-4-phenoxy-3-(3-thienylmethylthio)benzoic acid. After collection by filtration, recrystallisation from aqueous ethanol and drying, the compound is obtained with a melting point of 153°-155°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03972886 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-00902f74a4864767a5a0e349bd04017f |
| Source note | uspto-grants-1976_08 |