HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → t-Butyl 3-methyl-4-nitrophenoxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methyl-4-nitrophenol | HCID 17412 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | t-Butyl 3-methyl-4-nitrophenoxyacetate | HCID 23370041 | — |
Reaction Steps
In a similar manner to Example 2, starting material step (b), t-butyl bromoacetate (2.9 ml), 3-methyl-4-nitrophenol (2.5 g), anhydrous potassium carbonate (2.7 g) and acetone (100 ml) were reacted to give t-butyl 3-methyl-4-nitrophenoxyacetate (4.19 g) as an off-white solid: NMR Spectrum (DMSO-d6) 1.44 (9H, s), 2.56 (3H, s), 4.71 (2H, s), 6.94 (1H, dd), 7.03 (1H, d), 8.06 (1H, d); Mass Spectrum m/Z 268 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576334 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-622d88387a0543aab073dc1ddbdbcdb6 |
| Source note | uspto-grants-1996_11 |