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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281077Generated: October 31, 2026

Chloroacetic Acid → Uracil-5-ylacetic acid

https://huagongshe.com/reaction/1281077

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 numberUS06451968B1
Source datasetuspto-grants-2002_09
ORD IDord-8f8ff3d0fb3842aa9caa3190ccf5cae0
Source noteuspto-grants-2002_09