HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2-Cyclohexyl-5-methyl-oxazol-4-yl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2-Cyclohexyl-5-methyl-oxazol-4-yl)-acetonitrile | HCID 15343904 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | (2-Cyclohexyl-5-methyl-oxazol-4-yl)-acetic acid | HCID 10857080 | — |
Reaction Steps
1.900 g of the above prepared (2-cyclohexyl-5-methyl-oxazol-4-yl)-acetonitrile (9.30 mmol) was dissolved in 21 ml EtOH/water=1/1 and treated with 5 eq. of NaOH-pellets (1.86 g). Hydrolysis was allowed to proceed over night at 60° C. After cooling, 25% HCl was added, followed by AcOEt. After separation of the two layers, the aq. phase was again extracted with AcOEt, the combined organic layers washed with water, dried over sodium sulfate, and evaporated to dryness to yield 1.920 g of the title acid as light-brown, waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109225B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-e2db40434a7e4513900f2ab5d9b25702 |
| Source note | uspto-grants-2006_09 |