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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester

4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester

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4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester Basic information

Product Name:
4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
Synonyms:
  • 4-ACETYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 1-N-Boc-4-Acetylpiperidine
  • N-Boc-4-acetylpiperidine
  • 1-tert-Butoxycarbonyl-4-acetylpiperidine
  • 1-Piperidinecarboxylic acid, 4-acetyl-, 1,1-dimethylethyl ester
  • 1-BOC-4-ACETYL-PIPERIDINE
  • N-Boc-4-Acetypiperidine
  • tert-Butyl 4-acetylpiperidine-1-carboxylate
CAS:
206989-61-9
MF:
C12H21NO3
MW:
227.3
Mol File:
206989-61-9.mol
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4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester Chemical Properties

Boiling point:
312.4±35.0 °C(Predicted)
Density 
1.052±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-2.23±0.40(Predicted)
InChI
InChI=1S/C12H21NO3/c1-9(14)10-5-7-13(8-6-10)11(15)16-12(2,3)4/h10H,5-8H2,1-4H3
InChIKey
HNVBBNZWMSTMAZ-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)CCC(C(C)=O)CC1
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
HazardClass 
IRRITANT
HS Code 
2933399990
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4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester Usage And Synthesis

Appearance

Light yellow oil

Uses

tert-Butyl 4-Acetylpiperidine-1-carboxylate is a useful research chemical.

Synthesis

Tert-butyl-4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate (2.29 g, 8.32 mmol) was dissolved in 30 ml of tetrahydrofuran (THF), and the resulting solution was cooled to -78 °C. To the solution, methylmagnesium bromide (3.0 M) (7.73 ml, 10.82 mmol) was slowly added, and the solution was stirred at 0 °C for 1 hr. After the reaction was completed with a 2 N hydrochloric acid aqueous solution, 6 N sodium hydroxide solution was added to adjust the pH to 10. Then the solution was extracted with dichloromethane. The organic layer was treated with magnesium sulfate (MgSO4) and filtered, and the solution was concentrated. The resulting residue was isolated and purified by silica gel column chromatography (dichloromethane/methanol = 10/1) to give 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester (6.36 g, 94.0 percent).

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