HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → HCID 14457166, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14457167 | HCID 14457167 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14457166 | HCID 14457166 | — |
Reaction Steps
A mixture of 8.65 g of the product of Step A in 130 ml of toluene, 2.8 g of potassium hydroxide, 4.5 ml of 3-bromo-1-propyne and 1.66 g of tetrabutyl ammonium bromide was heated to 95 C and stirred for 3 hours. The mixture was decanted, washed with N sodium hydroxide, with N hydrochloric acid and with water saturated with sodium chloride, dried and brought to dryness. The residue was chromatographed and elution with a hexane-chloroform-acetone mixture (70-15-15) yielded 4.74 g of the expected product melting at 70° to 71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008281 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-66a19989a7d04eb99f52703e0c477e2c |
| Source note | uspto-grants-1991_04 |