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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508588Generated: October 31, 2026

Hydrochloric Acid → HCID 68075485, compound

https://huagongshe.com/reaction/1508588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantLithium tritertbutoxyaluminohydrideHCID 16684435—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 68080597HCID 68080597—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68075485HCID 68075485—

Reaction Steps

Lithium tri-tert-butoxyaluminohydride (13.78 g, 54.2 mmol) was added into a cold (dry ice/acetone bath) solution of benzyl {(2S)-1-oxo-1-[3-(trifluoromethoxy)phenyl]propan-2-yl}carbamate (3.98 g, 10.84 mmol) in ethanol (100 ml). LCMS indicated the reaction was completed in 10 min. The reaction was quenched by HCl (1N). The crude mixture was diluted w/ ethyl acetate and filtered through a bed of Celite® 521 (slow filtration). Volatiles were removed from the filtrate under reduced pressure. The resulting pot residue was worked up with aqueous sodium hydrogen carbonate/brine, extracted with ethyl acetate, dried over Na2SO4, filtered and evaporated to afford a white solid. This solid was stirred with potassium hydroxide (7.22 ml, 54.2 mmol) in a THF (100 ml)/methanol (50 ml) mixture at room temperature for 2 hrs. LCMS indicated completion of reaction. HCl (1N) was added to acidify the reaction mixture. Volatiles were removed under reduced pressure. The pot residue was worked up with brine, extracted with ethyl acetate, dried over Na2SO4, filtered and evaporated to afford a dark mixture. The resulting crude mixture was purified by flash chromatography (SiO2, Biotage 65i cartridge). The column was eluted by an ethyl acetate/hexanes mixture (0% to 100% ethyl acetate). Related fractions were pooled and evaporated to a white solid of 1.4170 g as the titled compound. LCMS calc.=261.06. found=260.21 (M−1)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221834B2
Source datasetuspto-grants-2015_12
ORD IDord-c0e1aec7cf1846d6aa0c386bc225786e
Source noteuspto-grants-2015_12