HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920530Generated: October 30, 2026
Potassium Hydroxide → HCID 86670009, compound
https://huagongshe.com/reaction/920530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86670010 | HCID 86670010 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86670009 | HCID 86670009 | 93.4% |
Reaction Steps
To a solution of methanesulfonic acid 4-(2-bromo-acetyl)-3-trifluoromethyl-phenyl ester (33.95 g; 89.3 mmol) in 1,4-dioxane (150 mL) was added dropwise a solution of NaBH4 (2.37 g; 62.5 mmol) in water (47 mL). The resulting mixture was stirred at RT for 2.5 hours, subsequently, quenched with 0.5M aqueous HCl (125 mL), and extracted with EtOAc. The combined organic layers were washed with water, dried (MgSO4), filtered and concentrated in vacuo. The residue was dissolved in Et2O (500 mL) and treated with a solution of KOH (4.19 g; 74.7 mmol) in water (100 mL). The resulting mixture was heated under reflux for 4 hours. After cooling to RT, the volatiles were removed in vacuo and the residue was partitioned between EtOAc and water. The organic layer was washed with water, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (CH2Cl2) to afford methanesulfonic acid 4-oxiranyl-3-trifluoromethyl-phenyl ester (23.54 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273017B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-2db02ea680bb4c30a03e9bf5b3c5b241 |
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| Source note | uspto-grants-2016_03 |
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