HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → (3E)-4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | I2-Ionone | HCID 638014 | — |
| Product | (3E)-4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-ol | HCID 5373729 | — |
Reaction Steps
β-Ionol was synthesized from β-ionone as described above for synthesis for aα-ionol with the following modification: 20% sodium hydroxide solution was used to hydrolyze the reaction complex in place of the sulfuric acid solution and the separated organic layer was neutralized by washing with water. α-Ionol thus prepared had the following constants: boiling point, 78° C./0.2 mm; nD25 1.4975; yield 5.9 g. Infrared spectrum and GC retention time was identical to that of a commercially available sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877607 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-f06844a67396475bbaee383b72ced181 |
| Source note | uspto-grants-1989_10 |