Basic information Safety Supplier Related

1-N-Boc-2-Methylhydrazine

Basic information Safety Supplier Related

1-N-Boc-2-Methylhydrazine Basic information

Product Name:
1-N-Boc-2-Methylhydrazine
Synonyms:
  • 2-Methylhydrazinecarboxylic acid tert-butyl ester
  • 1-N-Boc-2-Methylhydrazine
  • 1-(t-butyloxy)carbonyl-2-Methylhydrazine
  • Hydrazinecarboxylic acid, 2-Methyl-, 1,1-diMethylethyl ester
  • 1-(t-butylo×y)carbonyl-2-Methylhydrazine
  • tert-butyl 2-Methylhydrazinecarboxylate
  • 2-Methylhydrazinecarboxylic acid tert-butyl est
  • tert-butyl 2-methylhydrazine-1-carboxylate
CAS:
127799-54-6
MF:
C6H14N2O2
MW:
146.19
Mol File:
127799-54-6.mol
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1-N-Boc-2-Methylhydrazine Chemical Properties

Melting point:
49-51℃
Density 
0.982±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
10.73±0.43(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C6H14N2O2/c1-6(2,3)10-5(9)8-7-4/h7H,1-4H3,(H,8,9)
InChIKey
UZRUVUYVHGPEAP-UHFFFAOYSA-N
SMILES
N(C(OC(C)(C)C)=O)NC
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Safety Information

HS Code 
2928009090
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1-N-Boc-2-Methylhydrazine Usage And Synthesis

Synthesis

127799-53-5

127799-54-6

The general procedure for the synthesis of 1-Boc-2-methylhydrazine from 1-Cbz-2-Boc-1-methylhydrazine is as follows: 24.8 g (70.8 mmol) of 1-benzyl-2-tert-butyl-1-methylhydrazine-1,2-dicarboxylate was dissolved in 500 mL of ethanol at room temperature and standard atmospheric pressure, and 1.24 g of palladium (10% activated charcoal) was added as a catalyst for the hydrogenation reaction. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth to remove the catalyst and the filtrate was concentrated and dried under reduced pressure to give the product. The yield was 12.3 g with a purity of 48%, representing 57% of the theoretical yield.

References

[1] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 16, p. 2297 - 2311
[2] Journal of the American Chemical Society, 1993, vol. 115, # 20, p. 8898 - 8906
[3] Tetrahedron Letters, 1996, vol. 37, # 2, p. 183 - 186
[4] Patent: US5030724, 1991, A
[5] Patent: US2016/52884, 2016, A1. Location in patent: Paragraph 0599-0600

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