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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880520Generated: November 3, 2026

Acetic Anhydride → HCID 57446943, compound

https://huagongshe.com/reaction/1880520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant5,5,5-trifluoroleucine HCl saltHCID 71359846—
SolventWaterHCID 962—
ProductHCID 57446943HCID 57446943—

Reaction Steps

To a cold (0° C.) solution of the 5,5,5-trifluoroleucine HCl salt (from Step 1 above) in H2O (30 mL) was added 1M aqueous NaOH (60 mL, 60 mmol) followed by acetic anhydride (3.5 mL, 36.7 mmol). The mixture was stirred at room temperature for 30 min to 1 h. After acidification with 6M aqueous HCl (6 mL), the mixture was extracted with EtOAc (6×). The combined EtOAc extracts were washed with brine, dried (MgSO4) and concentrated. The residue was swished with hexanes:Et2O (1:1) to afford N-acetyl-5,5,5-trifluoroleucine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318748B2
Source datasetuspto-grants-2012_11
ORD IDord-f0f903e0b30d47ed9366e198d1cc2648
Source noteuspto-grants-2012_11