HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 85700288, compound → HCID 14924162, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 85700288 | HCID 85700288 | — |
| Solvent | Potassium hydroxide methanol | HCID 23689386 | — |
| Product | HCID 14924162 | HCID 14924162 | 105.2% |
Reaction Steps
Ethyl 3-hydroxy-2-methylhept-6-enoate (6.11 g, 32.8 mmol) was dissolved in a 2 N potassium hydroxide-methanol solution (100 mL), and the mixture was stirred at room temperature for 2 hours and then left overnight. The methanol was distilled off under reduced pressure, and the residue was diluted with water, then washed with methylene chloride, and then neutralized with dilute hydrochloric acid. The aqueous layer was subjected to extraction with ethyl acetate, and the extract was washed with water and saturated saline and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a pale yellow oil (5.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947738B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-b35468e5cfb34401a74d074484572180 |
| Source note | uspto-grants-2011_05 |