HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244459Generated: October 27, 2026
Ammonium Chloride → 2-Cyclohexyl-2-hydroxy-2-thien-2-ylacetic Acid Methyl Ester
https://huagongshe.com/reaction/1244459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl alpha-oxo-2-thiopheneacetate | HCID 11217486 | — |
| Reactant | HCID 178478990 | HCID 178478990 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyclohexyl-2-hydroxy-2-thien-2-ylacetic Acid Methyl Ester | HCID 66959465 | — |
Reaction Steps
98.6 ml (0.197 mol) of a 2M solution of Cyclohexylmagnesium chloride in diethyl ether, were added to a solution of 27.97 g (0.164 mol) of 2-oxo-2-thien-2-ylacetic acid methyl ester dissolved in 370 ml of THF, at −78° C. under a N2 atmosphere. The mixture was stirred at this temperature for 10 minutes, and then warmed to room temperature. After 1 h, the reaction mixture was treated with a saturated solution of ammonium chloride and extracted three times with ethyl acetate. The organic phases were combined, washed with water, and dried over MgSO4. After removal of the solvent, the oil obtained was purified by column chromatography (silica gel) using hexane/AcOEt 90:10 as eluent. The yield was 16.2 g (39.5%) of a pure product, whose structure was confirmed by 1H-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122558B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-724a38349dea4c9e9a7ca8e0652fda8d |
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| Source note | uspto-grants-2006_10 |
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