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Methyl 6-(hydroxymethyl)nicotinate

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Methyl 6-(hydroxymethyl)nicotinate Basic information

Product Name:
Methyl 6-(hydroxymethyl)nicotinate
Synonyms:
  • 6-HYDROXYMETHYL-NICOTINIC ACID METHYL ESTER
  • METHYL 6-(HYDROXYMETHYL)NICOTINATE
  • 6-Hydroxymethyl-Nicotinic
  • methyl 6-(hydroxymethyl)nicotinate (en)
  • ethyl 6-(hydroxyMethyl)nicotinate
  • Methyl 6-(hydroxyMethyl)pyridine-3-carboxylate
  • 3-Pyridinecarboxylicacid, 6-(hydroxymethyl)-, methyl ester
  • Methyl 2-(hydroxyMethyl)pyridine-5-carboxylate
CAS:
56026-36-9
MF:
C8H9NO3
MW:
167.16
Product Categories:
  • Esters
  • Pyridines
Mol File:
56026-36-9.mol
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Methyl 6-(hydroxymethyl)nicotinate Chemical Properties

Melting point:
75-78℃
Boiling point:
293.4±30.0 °C(Predicted)
Density 
1.244±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
13.20±0.10(Predicted)
color 
White to Orange to Green
InChI
InChI=1S/C8H9NO3/c1-12-8(11)6-2-3-7(5-10)9-4-6/h2-4,10H,5H2,1H3
InChIKey
QVLONHSXRWCCAE-UHFFFAOYSA-N
SMILES
C1=NC(CO)=CC=C1C(OC)=O
CAS DataBase Reference
56026-36-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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Methyl 6-(hydroxymethyl)nicotinate Usage And Synthesis

Synthesis

881-86-7

56026-36-9

Step 1. Synthesis of methyl 6-(hydroxymethyl)nicotinate (55): a mixture of methyl 2,5-pyridinedicarboxylate (54; 100.0 g, 0.51 mol), CaCl2 (227.4 g, 2.05 mol), and THF (1100 mL) was mixed with EtOH (1200 mL), and stirred for 30 min. NaBH4 (48.6 g, 1.28 mol) was added in batches at 0 °C. The reaction mixture was stirred at room temperature for 18 hours. Subsequently, saturated NH4Cl solution (1.5 L) and water (2.0 L) were added slowly and extracted with dichloromethane (3 x 3.0 L). The organic phases were combined, dried with MgSO4 and concentrated under reduced pressure to give methyl 6-(hydroxymethyl)nicotinate 55 (82.0 g, 96% yield).

References

[1] Patent: WO2010/56549, 2010, A1. Location in patent: Page/Page column 103
[2] Journal of Organic Chemistry, 2010, vol. 75, # 3, p. 650 - 659
[3] Inorganic Chemistry, 2015, vol. 54, # 22, p. 10542 - 10558
[4] Patent: US2010/16373, 2010, A1. Location in patent: Page/Page column 16
[5] Patent: US2016/256578, 2016, A1. Location in patent: Paragraph 0124; 0125

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