HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaminophen → N-{4-[(5-Bromopentyl)oxy]phenyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaminophen | HCID 1983 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-{4-[(5-Bromopentyl)oxy]phenyl}acetamide | HCID 12355860 | 72.15% |
Reaction Steps
A solution of N-(4-hydroxyphenyl)-acetamide (paracetamol) (1) (1.50 g, 0.01 mol) and 1,5-dibromopentane (9) (10.0 ml) in ethyl methyl ketone (25.0 ml) containing potassium carbonate (5.0 g) was stirred for 8 hr at room temperature. The reaction mixture was filtered, residue washed with ethyl methyl ketone and solvent evaporated under reduced pressure to get the residue. The residue was dissolved in chloroform (200.0 ml), washed with 5% sodium hydroxide solution (3×100 ml), water (3×50 ml), dried, filtered and crystallized from methanol to get the desired product N-[4-(5-bromo-pentoxy)-phenyl]-acetamide (11) (2.15 g, 72.15%), mp 110-111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207222B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-c5d8c8f81a9045f3802240306d1ccb34 |
| Source note | uspto-grants-2012_06 |