HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 5-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 5-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid | HCID 57483804 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide | HCID 57483805 | 47.2% |
Reaction Steps
5-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid 9b (2.79 g, 11.97 mmol) was dissolved in 25 mL of dichloromethane followed by dropwise addition of boron tribromide (23.9 mL, 2.0 mol/L). The reaction mixture was reacted at room temperature for 1 hour. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was concentrated under reduced pressure after 5 mL of methanol was added. The residue was diluted with 100 mL of ethyl acetate and stirred for 1 hour. Then the mixture was filtered and the filter cake was dried to obtain the title compound 5-(3-amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide 9c (1.24 g, yield 47.2%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367710B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-d6f8238bd8944c7bbcd957a47474248d |
| Source note | uspto-grants-2013_02 |