4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE
4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE Basic information
- Product Name:
- 4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE
- Synonyms:
-
- 4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE
- Ethyl 4-Fluoropiperidine-4-carboxylate Hydrochloride
- Ethyl 4-fluoropiperidine-4-carboxylate, HCl
- Ethyl 4-fluoro-4-piperidinecarboxylate hydrochloride
- ethyl 4-fluoropiperidin-1-ium-4-carboxylate
- 4-Piperidinecarboxylic acid, 4-fluoro-, ethyl ester, hydrochloride (1:1)
- 4-fluoro-4-Piperidinecarboxylic acid ethyl ester hydrochloride (1:1)
- 4-Fluoro-4-piperidinecarboxylic acid ethyl ester HCl
- CAS:
- 845909-49-1
- MF:
- C8H15ClFNO2
- MW:
- 211.67
- Mol File:
- 845909-49-1.mol
4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- crystalline solid
- color
- White to off-white
4-FLUORO-4-PIPERIDINE ETHYLCARBOXYLATE HYDROCHLORIDE Usage And Synthesis
Uses
Ethyl 4-fluoropiperidine-4-carboxylate, HCl
Synthesis
416852-82-9
845909-49-1
General procedure for the synthesis of ethyl 4-fluoro-4-piperidinecarboxylate hydrochloride from ethyl N-Boc-4-fluoro-4-piperidinecarboxylate: To a solution of tert-butyl 4-chloro-4-tert-butyl-4-fluoro-piperidine-1,4-dicarboxylate (15 g, 54.48 mmol, 1.00 eq.) in methylene chloride (150 mL), a solution of 4 M hydrogen chloride in dioxane (100 mL) was added. The reaction mixture was stirred at 25 °C overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure to afford 11 g (95% yield) of ethyl 4-fluoropiperidine-4-carboxylate hydrochloride as a white solid.
References
[1] Patent: US2018/79742, 2018, A1. Location in patent: Paragraph 0328; 0329
[2] Patent: US2012/88750, 2012, A1. Location in patent: Page/Page column 34; 35
[3] Patent: US2018/258076, 2018, A1. Location in patent: Paragraph 0506
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