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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233553Generated: November 2, 2026

Ethyl Acetate → HCID 59296194, compound

https://huagongshe.com/reaction/2233553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 59296133HCID 59296133—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59296194HCID 5929619435.9%

Reaction Steps

458 mg Lithium aluminium hydride were suspended in 100 ml dry tetrahydrofuran and cooled in an ice bath. To this ice cooled suspension were added 4.5 g [5-Methyl-2-(4-pentafluorosulfanyl-phenyl)-thiazol-4-yl]-acetic acid ethyl ester, dissolved in 50 ml tetrahydrofuran. The reaction mixture was stirred for one hour. Then 300 ml ethyl acetate and 20 ml saturated NH4Cl solution were added. The organic layer was separated. The aqueous phase was extracted three times with portions of 50 ml ethyl acetate. The combined organic layers were dried over MgSO4 and the solvent was removed in vacuo. The residue was purified by flash chromatography with the eluent n-heptane:ethyl acetate=2:1 to provide 1.44 g 2-[5-methyl-2-(4-pentafluorosulfanyl-phenyl)-thiazol-4-yl]-ethanol as an oil which solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-2571f702e2df4449a084a47ed373b2a3
Source noteuspto-grants-2010_05