HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415684Generated: October 29, 2026
Water → [2-(4-Methoxyphenyl)-1,3-thiazol-4-yl]methanol
https://huagongshe.com/reaction/415684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate | HCID 10400532 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(4-Methoxyphenyl)-1,3-thiazol-4-yl]methanol | HCID 16494948 | 64.6% |
Reaction Steps
To an ice-cold suspension of LAH (0.08 g, 2.07 mmol) in 10 ml of anhydrous THF was added a solution of 2-(4-Methoxy-phenyl)-thiazole-4-carboxylic acid ethyl ester (0.26 g, 0.98 mmol) in 5 ml of THF. The reaction mixture was heated up to 60° C. for 1 h. After the completion of the reaction mixture (TLC monitoring), the reaction mixture was cooled to 0° C., water (2.0 ml) was added followed by the addition of 15% NaOH solution (2 mL) and finally 4 ml of water. The resulting solution was filtered through celite bed and concentrated under reduced pressure; water (25 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated to give the desired product (0.14 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088791B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-8657095d0c8c4d19b489d9c1b6e26850 |
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| Source note | uspto-grants-2012_01 |
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