HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-(Propargyloxy)-3,4-dimethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Dimethoxyphenol | HCID 16251 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Propargyloxy)-3,4-dimethoxybenzene | HCID 11252509 | — |
Reaction Steps
Following the same procedure as in Example 1, 13.8 g (0.1 mole) of 1-hydroxy-3,4-dimethoxybenzene, 13.8 g (0.1 mole) of anhydrous potassium carbonate in ml 50 of acetone and 14.9 g (0.1 mole) of a solution of propargyl bromide in toluene (80% w/w) were reacted. After work up and evaporation of the mixture u.v. (25° C./21 mbar) a residue was obtained that was purified on silica gel column (eluant n-hexane:ethyl acetate 5:1 v/v). A thick oil that after some time solidified with low melting point (28-30° C.) (b.p.: 109-110° C./ 3 mbar) was obtained whose NMR and MS analyses corresponded to those of the aforementioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809389B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-0602d7c0eb514623abff937009cc1986 |
| Source note | uspto-grants-2014_08 |