HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178471716, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 178468267 | HCID 178468267 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178471716 | HCID 178471716 | 89% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
400 mg (0.89 mmol) trans-4-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyrimidic acid ethyl ester were suspended in 10 ml water and heated to 100° C. for 2.5 h. EtOAc was added, and the inorganic phase was extracted with EtOAc. The combined organic phases were dried over Na2SO4 and evaporated to give 355 mg (89%) trans-4-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyric acid ethyl ester as yellow oil, MS: 452 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858651B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-382e7b4047244bfeab852808504e7b95 |
| Source note | uspto-grants-2005_02 |