6-Quinolinylmethanol

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6-Quinolinylmethanol manufacturers

  • 6-Quinolinylmethanol
  • 6-Quinolinylmethanol pictures
  • $1.00
  • 2019-07-06
  • CAS:100516-88-9
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 100KG
6-Quinolinylmethanol Basic information
Product Name:6-Quinolinylmethanol
Synonyms:RARECHEM AK ML 0560;4-cinnolinemethanol;6-quinolinemethanol;6-HYDROXYMETHYLQUINOLINE;6-QUINOLINYLMETHANOL;6-Hydroxymethylquinoline ,95%;6-Quinolinylmethanol ,97%;Quinoline-6-methanol
CAS:100516-88-9
MF:C10H9NO
MW:159.18
EINECS:
Product Categories:pharmacetical;Alcohols and Derivatives;Heterocycles
Mol File:100516-88-9.mol
6-Quinolinylmethanol Structure
6-Quinolinylmethanol Chemical Properties
Melting point 79-80 ºC
Boiling point 334.8±17.0 °C(Predicted)
density 1.218±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka14.02±0.10(Predicted)
AppearanceLight brown to yellow Solid
CAS DataBase Reference100516-88-9
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 6-24/25-26-36/37/39
HazardClass IRRITANT
HS Code 29334900
MSDS Information
6-Quinolinylmethanol Usage And Synthesis
Chemical PropertiesLight yellow or pink powder
Synthesis
METHYL QUINOLINE-6-CARBOXYLATE

38896-30-9

6-Quinolinylmethanol

100516-88-9

General procedure for the synthesis of 6-hydroxymethylquinoline from methyl 6-quinolinecarboxylate: cooling of a 0.2 M solution of methyl 6-quinolinecarboxylate (0.300 g, 1.60 mmol) in THF (8 mL) and a 0.6 M solution of diisobutylaluminum hydride (DIBAL) (0.860 mL, 4.81 mmol) in THF in an acetone-dry ice bath at -78 °C ( 8mL). The DIBAL solution was transferred to the methyl ester solution via cannula and the resulting solution was stirred for 1 h at 0 °C. The reaction was quenched by the addition of methanol (8 mL) and acetic acid (1.37 mL, 24.0 mmol) at 0 °C. After stirring for 5 min, saturated sodium tartrate solution (16 mL) was added. Stirring was continued for 20 min, followed by dilution of the reaction mixture with EtOAc (50 mL) and water (10 mL). The aqueous layer was extracted with EtOAc (3 x 50 mL). The organic phases were combined and washed once with 15 mL of water. The organic layer was dried with Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (50-90% EtOAc/hexane) afforded 0.236 g (93%) of 6-hydroxymethylquinoline (S3a) as a pale yellow oil.1H NMR (500 MHz, CDCl3): δ 4.89 (s, 2H), 7.35 (dd, 1H, J=4.0,8.0), 7.65 (dd, 1H, J=1.5, 9.0), 7.77 (s, 1H), 8.01 (d, 1H, J=9.0), 8.08 (d, 1H, J=4.0), 8.80 (dd, 1H, J=1.5,4.0).13C-NMR (125MHz, CDCl3): δ64.8,121.5,125.0,128.3,129.0,129.4. 136.4,139.9,147.7,150.2. HRMS-FAB (m/z): calculated value for [MH]+ C10H10NO, 160.0762; measured value: 160.0766.

References[1] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6404 - 6410
[2] Patent: WO2009/75778, 2009, A2. Location in patent: Page/Page column 49-50
[3] Patent: WO2004/7491, 2004, A1. Location in patent: Page 55-56
[4] Patent: WO2017/40449, 2017, A1. Location in patent: Paragraph 00363
[5] Patent: WO2011/18454, 2011, A1. Location in patent: Page/Page column 56
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