Basic information Safety Supplier Related

1-ETHYL-3-PYRROLIDINOL

Basic information Safety Supplier Related

1-ETHYL-3-PYRROLIDINOL Basic information

Product Name:
1-ETHYL-3-PYRROLIDINOL
Synonyms:
  • N-Ethyl-3-hydroxypyrrolidine
  • NSC 88610
  • 1-ethyl-3-hydroxy-terthydropyrrolo
  • 1-ethyl-3-pyrrolidino
  • 3-Pyrrolidinol, 1-ethyl-
  • 1-ETHYL-3-PYRROLIDINOL
  • 1-ETHYL-3-HYDROXYPYRROLIDINE
  • N-Ethylpyrrolidin-3-ol (racemat)
CAS:
30727-14-1
MF:
C6H13NO
MW:
115.17
EINECS:
250-310-7
Product Categories:
  • Heterocycles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrrolidines
Mol File:
30727-14-1.mol
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1-ETHYL-3-PYRROLIDINOL Chemical Properties

Boiling point:
59-61 °C1 mm Hg(lit.)
Density 
0.967 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.467(lit.)
Flash point:
165 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
pka
14.83±0.20(Predicted)
color 
Colorless to Brown
CAS DataBase Reference
30727-14-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
RTECS 
UY5685500
HS Code 
2933998090
Toxicity
mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02177,

MSDS

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1-ETHYL-3-PYRROLIDINOL Usage And Synthesis

Synthesis

2419-74-1

75-04-7

30727-14-1

The present embodiment is a method for the preparation of 1-ethyl-3-pyrrolidinol, which was carried out as follows: 250 g of 40 wt% aqueous ethylamine solution was added to a 500 mL four-necked flask, cooled to 10 °C, and placed in an ice-water bath. Under stirring conditions, 102 g of 1,4-dichloro-2-butanol was added dropwise, and the temperature was controlled to be about 15 °C. After the dropwise addition was completed in about 15 min, the reaction system was transferred to a 500 mL autoclave, sealed, evacuated to a pressure of 1.0±0.1 MPa, heated to 120±2°C, stirred and reacted for about 10 h. The reaction was monitored by GC until the raw material disappeared. After the reaction was completed, cooled to room temperature, discharged the reaction material, added 110g of sodium hydroxide in batches, taking care to control the temperature below 50°C to release ethylamine gas and precipitate a white solid, and continued stirring for 1h. After filtration, the filtrate was layered, the upper organic phase was taken, 100mL of ethanol and 18g of anhydrous magnesium sulfate were added, and stirred for 2~3h. Filtered again, and the filtrate was concentrated under vacuum to obtain a yellow transparent The filtrate was again filtered and concentrated under vacuum to obtain a yellow transparent oily liquid, and finally 46.7 g of colorless and transparent 1-ethyl-3-pyrrolidinol was obtained by vacuum distillation with a yield of 64.8% and a purity of 99.3% (HPLC).

References

[1] Patent: CN106631956, 2017, A. Location in patent: Paragraph 0022; 0023; 0024; 0025; 0026; 0027

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