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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | 1,2-Butanediol | HCID 11429 | — |
| Reactant | 4-Ethyl-1,3-dioxolane | HCID 121755 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68585259 | HCID 68585259 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(1-Hydroxymethylpropyloxy)-methyl-5-fluorouracil | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04415573 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-86475d75c42945d7b6a596c5f8ea7110 |
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| Source note | uspto-grants-1983_11 |
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