HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7633Generated: October 28, 2026
Water → Ethyl [(4-bromo-2-pyrimidinyl)thio]acetate
https://huagongshe.com/reaction/7633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 178418869 | HCID 178418869 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl [(4-bromo-2-pyrimidinyl)thio]acetate | HCID 12056458 | — |
Reaction Steps
Under argon, 52.5 g (0.20 mol) of triphenylphosphine are initially charged in 600 ml of dioxane, and 35.6 g (0.20 mol) of N-bromosuccinimide are added a little at a time, with cooling. The mixture is stirred at RT for 30 min. 8.6 g (0.04 mol) of ethyl [(4-hydroxy-2-pyrimidinyl)thio]acetate are then added and the mixture is heated at reflux for 45 min. A total of 2 l of water are added to the mixture, which is then extracted 3× with in each case 300 ml of methyl tert-butyl ketone. The organic phase is washed 2× with water and 1× with concentrated NaCl solution, dried over magnesium sulphate and concentrated. The residue is stirred in 60 ml of methyl tert-butyl ketone and filtered off. The mother liquor is concentrated and the residue is purified by silica gel chromatography (dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087616B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-7527eb69678f4b00afc468a3bbc062ef |
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| Source note | uspto-grants-2006_08 |
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