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5-[ethyl(2-hydroxyethyl)amino]pentan-2-one

CAS No.: 74509-79-8

product details:

Purity: 99%

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Cost-effective and customizable 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one 74509-79-8 in stock

  • Molecular Formula:C9H19 N O2
  • Molecular Weight:173.255
  • Vapor Pressure:0.000401mmHg at 25°C 
  • Boiling Point:282.2°C at 760 mmHg 
  • Flash Point:124.5°C 
  • PSA:40.54000 
  • Density:0.968g/cm3 
  • LogP:0.66980 

5-[ethyl(2-hydroxyethyl)amino]pentan-2-one(Cas 74509-79-8) Usage

Synthesis

30 g of N-ethylethanolamine, 1.2 g of tetrabutylammonium bromide, 25 g of potassium hydroxide, 240 g of chloroform,120g of water was added to the reaction flask, and then the temperature was controlled at 20 to 30 ° C, 38 g of 5-chloro-2-pentanone was added dropwise, and after the addition was completed, the mixture was stirred.Should be 3 hours, static layering, the water phase is discarded, the organic layer is added 24g anhydrous sodium sulfate, the temperature is controlled at 10 ~ 20 ° C, stirred and dried 1Hour, filtration, the filtrate is the organic phase of the condensation product, the content of which is detected, the condensation product is 51.7g, and the molar yield is 94.7% (to 5-Chloro-2-pentanone), GC purity ≧ 98.5%.

InChI:InChI=1/C9H19NO2/c1-3-10(7-8-11)6-4-5-9(2)12/h11H,3-8H2,1-2H3

74509-79-8 Relevant articles

HIGH-YIELDING CONTINUOUS FLOW SYNTHESIS OF ANTIMALARIAL DRUG HYDROXYCHLOROQUINE

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Page/Page column 19; 18, (2019/09/12)

Cost effective, semi-continuous flow met...

High-yielding continuous-flow synthesis of antimalarial drug hydroxychloroquine

Yu, Eric,Mangunuru, Hari P.R.,Telang, Nakul S.,Kong, Caleb J.,Verghese, Jenson,Gilliland, Stanley E.,Ahmad, Saeed,Dominey, Raymond N.,Gupton, B. Frank

supporting information, p. 583 - 592 (2018/03/21)

Numerous synthetic methods for the conti...

Side chain, synthesis method thereof, and method for synthesizing hydroxychloroquine sulfate from side chain

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Paragraph 0089; 0106; 0112; 0116; 0117; 0118; 0124, (2018/01/04)

The invention discloses a side chain, a ...

74509-79-8 Process route

5-chloro-2-pentanone
5891-21-4

5-chloro-2-pentanone

2-(Ethylamino)ethanol
110-73-6

2-(Ethylamino)ethanol

5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone
74509-79-8

5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone

Conditions
Conditions Yield
With tetrabutylammomium bromide; potassium hydroxide; In chloroform; water; at 20 - 30 ℃; for 3h;
94.7%
With sodium chloride; xylene;
5-iodo-2-pentanone
3695-29-2

5-iodo-2-pentanone

2-(Ethylamino)ethanol
110-73-6

2-(Ethylamino)ethanol

5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone
74509-79-8

5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone

Conditions
Conditions Yield
With potassium carbonate; In tetrahydrofuran; at 80 - 100 ℃; for 0.166667h; Flow reactor; Inert atmosphere;
86%
With potassium carbonate; In tetrahydrofuran; at 100 ℃; Flow reactor; Inert atmosphere;
14.05 g

74509-79-8 Upstream products

  • 5891-21-4
    5891-21-4

    5-chloro-2-pentanone

  • 110-73-6
    110-73-6

    2-(Ethylamino)ethanol

  • 3695-29-2
    3695-29-2

    5-iodo-2-pentanone

  • 517-23-7
    517-23-7

    3-acetyl-2-oxo-4,5-dihydrofuran

74509-79-8 Downstream products

  • 69559-11-1
    69559-11-1

    rac-5--2-pentanamine

  • 137433-23-9
    137433-23-9

    (S)-Hydroxychloroquine

  • 137433-23-9
    137433-23-9

    (R)-Hydroxychloroquine

  • 118-42-3
    118-42-3

    hydroxychloroquine

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