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Home > Encyclopedia > Ethyl 1-methyl-4-piperidinecarboxylate

Ethyl 1-methyl-4-piperidinecarboxylate

Ethyl 1-methyl-4-piperidinecarboxylate structure

Ethyl 1-methyl-4-piperidinecarboxylate 

structure
  • CAS No:

    24252-37-7

  • Formula:

    C9H17NO2

  • Chemical Name:

    Ethyl 1-methyl-4-piperidinecarboxylate

  • Synonyms:

    Ethyl 1-methylpiperidine-4-carboxylate;Ethyl 1-methyl-4-piperidinecarboxylate;1-Methyl-piperidine-4-carboxylic acid ethyl ester;Ethyl 1-methyl Piperidine-4-carboxylate;4-Piperidinecarboxylic acid, 1-methyl-, ethyl ester;ETHYL N-METHYLISONIPECOTATE;MFCD00130015;ethyl 1-methyl-piperidine-4-carboxylate;Ethyl N-methyl piperidine-4-carboxylate;1-methyl-4-piperidinecarboxylic acid ethyl ester

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

Colorless liquid

Ethyl 1-methyl-4-piperidinecarboxylate Basic Attributes

171.24

171.125931

2933399090

Characteristics

29.5

1

1.0±0.1 g/cm3

211°C at 760 mmHg

87℃

1.459

0.186mmHg at 25°C

Safety Information

NA 1993 / PGIII

3

37/38-41

26-36/37/39

Xi

P261-P280-P305 + P351 + P338

H315-H318-H335

Ethyl 1-methyl-4-piperidinecarboxylate Use and Manufacturing

Ethyl isonipecotate (20) (5.00 g, 31.8 nnno 1) was dissolved in an ice-cold mixture of glacial acetic acid (3.80 g, 63.6 mmol) and water (11 mL). Then, a 37percent aqueous formaldehyde solution (2.85 niL, 38.2 mmol) was added and the reaction mixture was hydrogenated over Pd/C (10percent, 338 mg) at 58 psi HReference 1-Methyl-piperidine-4-carboxylic acid hydrochloride; a) Preparation of 1-methyl-piperidine-4-carboxylic acid ethyl ester; Ethyl isonipecotate (3.0 g, 19.1 mmol) was added to a mixture of 90percent formic acid (10 mL) and 30percent aqueous formaldehyde (10 mL, 100 mmol) then the mixture was heated at reflux for 24 h. After cooling, the mixture was concentrated in vacuo to give an oil which was dissolved in dichloromethane. Solid sodium bicarbonate (1 g) was added and the mixture stirred for 1 h then filtered. The filtrate was concentrated in vacuo to afford 1-methyl-piperidine-4-carboxylic acid ethyl ester (2.0 g, 61percent) as a liquid, which was used as such for the next step.a)

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