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 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 |
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| Patent number | US07335687B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-8762e8a9462543b3ba7d0643fdd1663d |
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| Source note | uspto-grants-2008_02 |
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