Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178472355 | HCID 178472355 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178432839 | HCID 178432839 | 89.3% |
Reaction Steps
A mixture of cis/trans-4-(4,5-dimethyl-thiazol-2-yl)-cyclohexanecarboxylic acid ethyl ester (1:7) (170 mg, 0.636 mmol) in 1,4-dioxane (6.4 ml) and 2 M aqueous sodium hydroxide solution (3.2 ml, 6.4 mmol) was stirred for 24 h at room temperature. The reaction mixture was partitioned between ethyl acetate (25 ml) and water (25 ml). The aqueous layer was acidified to pH 4-5 by addition of 2 M aqueous hydrogen chloride solution (3.2 ml). The layers were separated. The aqueous layer was extracted with two 25-ml portions of ethyl acetate. The combined organic layers were washed with one 20-ml portion of brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound (136 mg, 89%) as white solid. MS m/e: 240 ([M−H]−)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513238B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c13c051e65a0428da63473e6c2e0e5a9 |
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| Source note | uspto-grants-2013_08 |
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