Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22404526 | HCID 22404526 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57195083 | HCID 57195083 | — |
Reaction Steps
10.00 Grams of the 2-chloro-4,6-dimethyl-1,5-heptadien-4-ol obtained above were dissolved in 94 g of N,N-dimethylformamide, and 9.65 g of potassium hydroxide in a flake form were added. The resultant mixture was stirred at room temperature for 4 hours and neutralized with a 20% acetic acid aqueous solution, and the resultant mixture was subjected to extraction with toluene. The toluene phase was washed with water and then dried over magnesium sulfate. The desiccant was filtered off, and then the toluene was distilled off under reduced pressure. The resultant oily substance was purified by silica gel column chromatography to give 6.32 g of methyl 2-methylallylpropargylcarbinol; nD25 =1.496, FI-MS m/e 138 (M+) (Propargyl compound/allene compound=100.0/0.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05258529 |
|---|
| Source dataset | uspto-grants-1993_11 |
|---|
| ORD ID | ord-dd83d773ca16424eaac1830cc58b3a27 |
|---|
| Source note | uspto-grants-1993_11 |
|---|