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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210902Generated: October 30, 2026

Acetic Acid → 1-Ethoxymethyl-5-ethyl-6-phenylthiouracil

https://huagongshe.com/reaction/2210902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantDiphenyl disulfideHCID 13436—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-Ethoxymethyl-5-ethyluracilHCID 10262317—
SolventEthyl AcetateHCID 8857—
Product1-Ethoxymethyl-5-ethyl-6-phenylthiouracilHCID 5446107032%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Then, 2.2 ml of lithium diisopropylamide (4.4 mmol) solution in tetrahydrofuran (2.1M) was added to 6 ml of tetrahydrofuran under a nitrogen atmosphere at -70° C., to which a solution of 0.40 g (2.0 mmol) of 1-ethoxymethyl-5-ethyluracil in 3 ml of tetrahydrofuran was added dropwise over 15 minutes. After stirring for 1 hour at -70° C., the reaction mixture was added with a solution of 0.57 g of diphenyl disulfide in 2 ml of tetrahydrofuran dropwise over 10 minutes and allowed to react for 30 minutes. The reaction mixture was added with 1 ml of acetic acid, brought to room temperature and then added with 30 ml of ethyl acetate. The mixture was washed with water (3 ml×5) and saturated aqueous solution of sodium hydrogencarbonate (twice), dried on magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/hexane=3:17) and crystallized from ethyl acetate to obtain 0.61 g of 1-ethoxymethyl-5-ethyl-6-phenylthiouracil (Yield: 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461060
Source datasetuspto-grants-1995_10
ORD IDord-1dd1befbb0ee4834b3be1dce481e2747
Source noteuspto-grants-1995_10