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DIETHYL (BOC-AMINO)MALONATE

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DIETHYL (BOC-AMINO)MALONATE Basic information

Product Name:
DIETHYL (BOC-AMINO)MALONATE
Synonyms:
  • LABOTEST-BB LT00452467
  • DIETHYL (BOC-AMINO)MALONATE
  • DIETHYL 2-[(TERT-BUTOXYCARBONYL)AMINO]MALONATE
  • DIETHYL 2-[N-(TERT-BUTOXYCARBONYL)AMINO]MALONATE
  • (boc-amino)malonic acid diethyl ester
  • (Boc-amino)malonic acid diethyl ester, Diethyl 2-[N-(tert-butoxycarbonyl)amino]malonate
  • Diethyl (Boc-aMino)Malonate,97%
  • Diethyl 2-[(tert-butoxycarbonyl)amino]malonate, Diethyl 2-[(tert-butoxycarbonyl)amino]propane-1,3-dioate
CAS:
102831-44-7
MF:
C12H21NO6
MW:
275.3
Product Categories:
  • Miscellaneous Reagents
  • Precursors for Amino Acid Synthesis
  • Building Blocks
  • C12 to C63
  • Carbonyl Compounds
  • Chemical Biology
  • Chemical Synthesis
  • Esters
  • Organic Building Blocks
  • Peptide Chemistry
Mol File:
102831-44-7.mol
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DIETHYL (BOC-AMINO)MALONATE Chemical Properties

Boiling point:
218 °C (lit.)
Density 
1.079 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.438(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,2-8°C
solubility 
Chloroform, Ethyl Acetate, Methanol
form 
Oil
pka
9.97±0.46(Predicted)
color 
Colourless
BRN 
5055305
Stability:
Below-40C
InChI
InChI=1S/C12H21NO6/c1-6-17-9(14)8(10(15)18-7-2)13-11(16)19-12(3,4)5/h8H,6-7H2,1-5H3,(H,13,16)
InChIKey
ULRLHEXGRUWQLQ-UHFFFAOYSA-N
SMILES
C(OCC)(=O)C(NC(OC(C)(C)C)=O)C(OCC)=O
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2917198090

MSDS

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DIETHYL (BOC-AMINO)MALONATE Usage And Synthesis

Chemical Properties

Colourless Oil

Uses

Diethyl (Boc-amino)malonate (cas# 102831-44-7) is a compound useful in organic synthesis.

Synthesis

6829-40-9

24424-99-5

102831-44-7

Diethyl aminomalonate (17.5 g, 0.1 mol) and triethylamine (20 g, 0.2 mol) were dissolved in 250 mL of dichloromethane in a three-necked flask under ice bath conditions. Subsequently, di-tert-butyl dicarbonate (26 g, 0.12 mol) was slowly added. The reaction mixture was gradually brought to room temperature and stirred continuously at this temperature and the progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was extracted with dichloromethane (200 mL × 3). The organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated to give 27 g of the colorless oily product diethyl 2-Boc-aminomalonate in 98% yield.

References

[1] Journal of Organic Chemistry, 1986, vol. 51, # 15, p. 2910 - 2913
[2] Patent: CN106946724, 2017, A. Location in patent: Paragraph 0027; 0028; 0034; 0040
[3] Bioorganic and Medicinal Chemistry, 2002, vol. 10, # 12, p. 3973 - 3979
[4] Journal of Medicinal Chemistry, 2009, vol. 52, # 9, p. 2909 - 2922
[5] Patent: US2003/65176, 2003, A1

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