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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247080Generated: October 25, 2026

Triethylamine → 1-(3-Methylphenylthio)methyl-5-fluoropyrimidin-2-one

https://huagongshe.com/reaction/247080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Fluoropyrimidin-2-oneHCID 101498—
ReactantPotassium BromideHCID 253877—
Reactant3-Methylphenyl chloromethyl sulfideHCID 12840894—
SolventDichloromethaneHCID 6344—
Product1-(3-Methylphenylthio)methyl-5-fluoropyrimidin-2-oneHCID 15650500—

Reaction Steps

3-(Chloromethylthio)toluene (6.5 mmol) was added to a solution of 5-fluoropyrimidin-2-one (6.5 mmol) and triethylamine (6.5 mmol) in dichloromethane (75 ml) and the resultant mixture heated under reflux for 2 days. The solvent was then distilled off, the residue triturated with water and the residual material extracted with CCl4. Evaporation of the extracts and crystallisation of the residue from ethyl acetate gave the pure product; 0.40 g (25%), m.p. 124° C. (Found: C57.42; H4.63. Calc. for C12H11FN2OS: C57.59; H4.43) 1H NMR (DMSO d6); δ 2.28 (Me), 5.17(CH2), 7.2 (Ph), 8.05 (H-4), 8.70 (H-6). IR (KBr): 1670 cm-1 (CO), MS [70 eV, m/z (% rel. int.)]: 250 (8,M), 137(11), 136(36), 135(10), 128(7), 127(100), 100(34), 91(9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705791
Source datasetuspto-grants-1987_11
ORD IDord-be950a6fa23d444c879577fb33e2a1e5
Source noteuspto-grants-1987_11