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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 178418869HCID 178418869—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl [(4-bromo-2-pyrimidinyl)thio]acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087616B2
Source datasetuspto-grants-2006_08
ORD IDord-7527eb69678f4b00afc468a3bbc062ef
Source noteuspto-grants-2006_08