Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079773Generated: October 31, 2026

Ammonium Chloride → Ethyl 2-(methylthio)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/2079773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
ProductEthyl 2-(methylthio)pyrimidine-5-carboxylateHCID 10442716—

Reaction Conditions

Temperature80 °C

Reaction Steps

Ethyl 4-chloro-2-methylthio-5-pyrimidine carboxylate (12.5 g, 53.88 mmol) and Zn powder (14.1 g, 215.52 mmol) were combined and benzene (60 ml) and 3M NH4Cl (140 ml) were added. The suspension was stirred vigorously and heated to 80° C. for 30 h. The reaction mixture was filtered through celite and washed with EtOAc (200 ml). The filtrate was concentrated in vacuo to about 50 ml and then partitioned between H2O (400 ml) and EtOAc (400 ml). The aqueous layer was further extracted with EtOAc (250 ml). The combined organic layers were dried (MgSO4) and concentrated in vacuo to a dark oil. This was purified by column chromatography eluting with neat heptane followed by 1:1:1 heptane/CH2Cl2/Et2O and finally 2:2:0.5 heptane/CH2Cl2/Et2O. The title compound was obtained as a colourless oil (13 g, 61%). m/z 199 [M+H]+, 1H NMR (300 MHz, d6-DMSO) δ: 1.30 (3H, t), 2.60 (3H, s), 4.35 (2H, q), 9.0 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932246B2
Source datasetuspto-grants-2011_04
ORD IDord-b3d2e732d58847778d0f34e256f7373a
Source noteuspto-grants-2011_04