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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305985Generated: November 1, 2026

Chloroacetic Acid → Uracil-5-ylacetic acid

https://huagongshe.com/reaction/2305985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl (4-oxo-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-5-yl)acetateHCID 3659581—
SolventWaterHCID 962—
ProductUracil-5-ylacetic acidHCID 298035—

Reaction Steps

Ethyl (2-thiouracil-5-yl)acetate (33, 7.8 g, 36 mmol) was mixed with chloroacetic acid (1.9 g, 20 mmol) and water (47 ml) and refluxed for 2 hours. Concentrated hydrochloric acid (22 ml) was added and the reaction mixture was refluxed overnight. The reaction mixture was filtered and the precipitate was washed once with water and dried. The procedure was repeated with the precipitate in place of 8 yielding 4.19 g (68%) of the title compound as a white solid. 1H-NMR (DMSO-d6/TMS): 2=3.13 (s, 2H, CH2COO); 7.35 (d, 1H, J=6.5 Hz, H-6); 10.74 (m, 1H, H-1); 11.09 (s, 1H, H-3); 12.20 (br, 1H, COOH). 13C-NMR (DMSO-d6/TMS): δ=31.3 (CH2COO); 106.6 (C-5); 139.7 (C-6); 151.2 (C-2); 164.0 (C-4); 171.9 (COOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441130B1
Source datasetuspto-grants-2002_08
ORD IDord-e6797ea3aa634fca88abdc78f4da6e93
Source noteuspto-grants-2002_08