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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881793Generated: November 1, 2026

Uracil → 3,5-Dioxohexanoic acid

https://huagongshe.com/reaction/881793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUracilHCID 1174—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3,5-Dioxohexanoic acidHCID 5459844—

Reaction Steps

N,O-Bis(trimethylsilyl)acetamide (BSA, 54.7 mL, 224 mmol) was added to a stirred suspension of uracil (10.2 g, 90.7 mmol) and Compound 54 (31.1 g, 60.4 mmoles) in dry acetonitrile (300 mL). After stirring at rt for 30 min a clear solution was observed, and the reaction was cooled to 0° C. under nitrogen. Trimethylsilyfluoromethanesulfonate (TMSOTf, 21.9 mL, 121 mmol) was added and after the reaction was stirred at rt for 15 min, it was transferred to a preheated oil bath at 80° C. After stirring for 4 h at 80° C., the reaction was cooled to rt and MeO H (20 mL), EtOAc (250 mL) and H2O (400 mL) were added. The organic phase was then sequentially washed with sat. NaHCO3, brine, dried (Na2SO4) and concentrated to provide the crude triacetate. TLC (Rf═0.60, 80% EtOAc/hexanes). LCMS (Method m/z═567.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993738B2
Source datasetuspto-grants-2015_03
ORD IDord-a8617aaaf81e43a8aaa35b1780aca161
Source noteuspto-grants-2015_03