DIETHYL (BOC-AMINO)MALONATE
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
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
MSDS
- Language:English Provider:SigmaAldrich
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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