HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508158Generated: October 25, 2026
Water → [2-(4-Chloro-3-methylphenyl)-1,3-oxazol-4-yl]methanol
https://huagongshe.com/reaction/508158
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 2-(4-chloro-3-methylphenyl)-1,3-oxazole-4-carboxylate | HCID 58284444 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(4-Chloro-3-methylphenyl)-1,3-oxazol-4-yl]methanol | HCID 58284347 | — |
Reaction Steps
46 mg (1.22 mmol) of lithium aluminum hydride are initially charged in 8.0 ml of THF and cooled to 0° C. A solution of 161 mg (0.61 mmol) of the compound from Example 26A in 2.5 ml of THF is then added dropwise. The mixture is stirred at RT for 2 h. The reaction solution is then once more cooled to 0° C., and 0.2 ml of water and 0.4 ml of 1 N aqueous sodium hydroxide solution are added. The mixture is stirred at RT overnight. The precipitate formed is filtered off, and the filtrate is freed from the solvent using a rotary evaporator. The residue is used without further purification in the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09095582B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-1416c1ca9a0c43d886b805592fc7c512 |
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| Source note | uspto-grants-2015_08 |
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