HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetic Acid → 2-alpha-Bromoacetamido-4-benzyloxyphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | 2-Amino-4-(benzyloxy)phenol | HCID 14169807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-alpha-Bromoacetamido-4-benzyloxyphenol | HCID 53699943 | 505.7% |
Reaction Steps
Bromoacetic acid (13.9 g, 0.01 mole) and dicyclohexyldicarbodiimide (DCCD, 20.6 g, 0.01 mole) were added at room temperature under stirring to the amine ((b), 21.5 g, 0.01 mole) in THF (200 ml). After 1 hour the reaction mixture was filtered and the liquid evaporated to dryness under vacuum. The residue was crystallized from acetic acid (50 ml) to give the bromoamide ((c), 17 g, 50%) as white prisms. The product strusture was confirmed by NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04672013 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-6024578013d44cae916d3f1bbdfe21c1 |
| Source note | uspto-grants-1987_06 |