HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tyramine → 6-Bromo-N-[2-(4-hydroxyphenyl)ethyl]-hexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tyramine | HCID 5610 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromohexanoic acid | HCID 20210 | — |
| Reactant | Di(succinimido) carbonate | HCID 676246 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Bromo-N-[2-(4-hydroxyphenyl)ethyl]-hexanamide | HCID 19080235 | — |
Reaction Steps
To a solution of 6-bromohexanoic acid (4.51 g, 23.1 mmol) in acetonitrile (50 mL) is added N,N'-disuccinimidyl carbonate (6.5 g, 25 mmol) and triethylamine (3.2 mL, 23 mmol). The solution is stirred at room temperature for 4 hours and tyramine (3.2 g, 23 mmol) is added and stirred continued at room temperature overnight, evaporated in vacuo, re-dissolved in ethyl acetate (100 mL) and washed with water (6×50 mL) and saturated sodium chloride solution (2×25 mL). The ethyl acetate solution is dried with sodium sulfate, filtered, and evaporated in vacuo to give a light brown gum. The crude product is purified by silica gel chromatography to give 6-bromo-N-[2-(4-hydroxyphenyl)ethyl]-hexanamide (II) as a light amber syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688966 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-3c003b99891d49e5a0e1514eb5ffdd81 |
| Source note | uspto-grants-1997_11 |