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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649106Generated: November 2, 2026

5-Fluorouracil → 1-(1-Hydroxymethylpropyloxy)-methyl-5-fluorouracil

https://huagongshe.com/reaction/1649106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouracilHCID 3385—
Reactant1,2-ButanediolHCID 11429—
Reactant4-Ethyl-1,3-dioxolaneHCID 121755—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68585259HCID 68585259—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product1-(1-Hydroxymethylpropyloxy)-methyl-5-fluorouracilHCID 20480603—

Reaction Steps

4-Ethyl-1,3-dioxolane (10 ml) prepared from butane-1,2-diol was added to bis(trimethylsilyl)-5-fluorouracil prepared from 5-fluorouracil (10 g) as in Example 1. To the mixture was added dropwise a solution of anhydrous stannic chloride (6 ml) in chloroform (15 ml) over one hour under cooling in an ice bath followed by stirring at room temperature for one hour. The reaction mixture was poured into methanol (100 ml) containing sodium bicarbonate (30 g), and after removing the resulting precipitate, the filtrate was evaporated under reduced pressure. The residue was dissolved in water (10 ml), purified by column chromatography with use of Amberlite XAD-4 (Rohm and Haas Co.), and treated with benzene to give 6.9 g of crystalline 1-(1-hydroxymethylpropyloxy)-methyl-5-fluorouracil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415573
Source datasetuspto-grants-1983_11
ORD IDord-86475d75c42945d7b6a596c5f8ea7110
Source noteuspto-grants-1983_11