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2-(Chloromethyl)pyrimidine

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2-(Chloromethyl)pyrimidine Basic information

Product Name:
2-(Chloromethyl)pyrimidine
Synonyms:
  • PYRIMIDINE, 2-(CHLOROMETHYL)-
  • 2-(CHLOROMETHYL)-PYRIMIDINE
  • Pyrimidine, 2-(chloromethyl)- (9CI)
  • 2-(chloromethyl)pyrimidine(SALTDATA: HCl)
  • 2-(Chloromethyl)pyrimidin...
  • 2-chloroMrthyl pyriMidine
  • 2-(ChloroMethyl)pyriMidine(HCl ForM)
  • 2-Chlormethyl-pyrimidin
CAS:
54198-88-8
MF:
C5H5ClN2
MW:
128.56
Product Categories:
  • PYRIMIDINE
  • Heterocycle-Pyrimidine series
Mol File:
54198-88-8.mol
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2-(Chloromethyl)pyrimidine Chemical Properties

Boiling point:
101-103 °C(Press: 26 Torr)
Density 
1.241±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
0.43±0.13(Predicted)
form 
liquid
color 
Brown
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Safety Information

HS Code 
2933998090
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2-(Chloromethyl)pyrimidine Usage And Synthesis

Synthesis

42839-09-8

54198-88-8

General procedure for the synthesis of 2-(chloromethyl)pyrimidine from 2-pyrimidine methanol: To a stirred solution of pyrimidin-2-ylmethanol (4.5 g, 40.90 mmol) in dichloromethane (DCM, 50 mL) was slowly added thionyl chloride (SOCl2, 10 mL) at 0 °C and protected by an inert atmosphere. The reaction mixture was gradually warmed to 50 °C and stirred continuously for 2 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the complete conversion of the feedstock, the volatiles were removed by distillation under reduced pressure. The residue was quenched with ice-cold water and subsequently neutralized with saturated sodium bicarbonate (NaHCO3) solution and extracted with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography to afford 2-(chloromethyl)pyrimidine in brown liquid form (960 mg, 18% yield). The product was characterized as follows: 1H-NMR (DMSO-d6, 400 MHz): δ8.84 (d, 2H), 7.52 (t, 1H), 4.82 (s, 2H); Mass spectrometry (ESI): m/z 128.5 [M + 1]+; Liquid Chromatography-Mass Spectrometry (LC-MS) purity: 95.09% (column: Chromolith RP-18, 100×4.6 mm; retention time: 3.86 min; mobile phase: 5 mM NH4OAc/acetonitrile (ACN); flow rate: 0.8 mL/min); thin-layer chromatography (TLC) conditions: 70% ethyl acetate/hexane (Rf value: 0.6).

References

[1] Patent: WO2012/40230, 2012, A1. Location in patent: Page/Page column 81
[2] Patent: US4118567, 1978, A
[3] Patent: EP150984, 1991, B1
[4] Patent: US4826833, 1989, A
[5] Patent: WO2013/142269, 2013, A1. Location in patent: Paragraph 0509; 0510

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