Basic information Safety Supplier Related

Ethyl 4-hydroxypiperidine-1-carboxylate

Basic information Safety Supplier Related

Ethyl 4-hydroxypiperidine-1-carboxylate Basic information

Product Name:
Ethyl 4-hydroxypiperidine-1-carboxylate
Synonyms:
  • 1-(Ethoxycarbonyl)piperidin-4-ol
  • N-Carboethoxypiperidine-4-Ol
  • N-carbethoxy-4-piperidinemethanol
  • N-carbethoxy-4-hydroxypiperidone.
  • Ethyl 4-hydroxypiperidine-1-caroxylate
  • Ethyl 4-hydroxy-N-piperidinecarboxylate
  • 1-Ethoxycarbonyl-1-piperidinol, 98%
  • Ethyl 4-hydroxypiperidine-1-ca
CAS:
65214-82-6
MF:
C8H15NO3
MW:
173.21
EINECS:
265-636-5
Product Categories:
  • Piperidine
Mol File:
65214-82-6.mol
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Ethyl 4-hydroxypiperidine-1-carboxylate Chemical Properties

Boiling point:
120-130 °C(Press: 0.098 Torr)
Density 
1.12
refractive index 
1.4802
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
pka
14.80±0.20(Predicted)
color 
Colorless to Light yellow to Light orange
InChI
InChI=1S/C8H15NO3/c1-2-12-8(11)9-5-3-7(10)4-6-9/h7,10H,2-6H2,1H3
InChIKey
QABJNOSERNVHDY-UHFFFAOYSA-N
SMILES
N1(C(OCC)=O)CCC(O)CC1
CAS DataBase Reference
65214-82-6(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
HS Code 
29333990
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Ethyl 4-hydroxypiperidine-1-carboxylate Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

Ethyl 4-hydroxypethidine-1-carboxylate is mainly used as a pharmaceutical intermediate and a raw material for organic matter. It can be used in the synthesis of antihistamines, antipsychotics, antidepressants, and various pesticides. As an intermediate, the compound can also produce fungicides and insecticides. It can be used as a raw material for synthetic surfactants, flavors, and fragrances.

Preparation

Add triethylamine (1.5 equivalent) and ethyl chlorine 4-hydroxypiperidine-1-carboxylate (1.2 equivalent) to the dichloromethane solution of 4-hydroxypiperidine (1.0 equivalent) at 0 °C. Stir the mixture at 0 °C for 30 min. The reaction mixture is then poured into water and extracted with methylene chloride. Wash organic extracts with water and salt water. The compound is placed on sodium sulfate to dry. Finally, the organic extract is concentrated under reduced pressure to obtainEthyl 4-hydroxypiperidine-1-carboxylate.

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