HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 15-Hydroxy-12-ketopentadecanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-(11-Cyanoundecanoyl)-gamma-butyrolactone | HCID 11747922 | — |
| Product | 15-Hydroxy-12-ketopentadecanoic acid | HCID 9881955 | 93.3% |
Reaction Steps
279 g (1.00 millimole) of α-(11-cyanoundecanoyl)-γ-butyrolactone, 0.68 g (10.3 millimole) of 85% potassium hydroxide and 5.66 g of water were charged and heated under reflux over 10 hours. After completion of the reaction, the system was cooled and made acidic by use of 5 ml of 4N-HCl, followed by extraction once from 70 ml of methylene chloride and two times from 20 ml of the same. After the methylene chloride solution was dried over sodium sulfate, concentration was conducted to dryness to obtain white solid. The obtained white solid was purified with use of a silicagel column by using n-hexane/ethyl acetate (1:1, volume ratio) as a developer to obtain 0.254 g (0.933 millimole, yield: 93 %) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05099036 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-347963d26d1e45259d86a3da433e0657 |
| Source note | uspto-grants-1992_03 |