Basic information Safety Supplier Related

tert-butyl 3-bromoazetidine-1-carboxylate

Basic information Safety Supplier Related

tert-butyl 3-bromoazetidine-1-carboxylate Basic information

Product Name:
tert-butyl 3-bromoazetidine-1-carboxylate
Synonyms:
  • tert-butyl 3-bromoazetidine-1-carboxylate
  • 1-Boc-3-broMoazetidine
  • 3-Bromo-1-azetidinecarboxylic acid tert-butyl ester
  • N-Boc-3-BroMoazetidine
  • 1-Azetidinecarboxylic acid, 3-bromo-, 1,1-dimethylethyl ester
  • 1-Boc-3-bromoazetidine - [B7997]
CAS:
1064194-10-0
MF:
C8H14BrNO2
MW:
236.11
Mol File:
1064194-10-0.mol
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tert-butyl 3-bromoazetidine-1-carboxylate Chemical Properties

Boiling point:
258℃
Density 
1.443
Flash point:
110℃
storage temp. 
2-8°C
pka
-3.76±0.40(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C8H14BrNO2/c1-8(2,3)12-7(11)10-4-6(9)5-10/h6H,4-5H2,1-3H3
InChIKey
RUTPPPNQDPSSBM-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)CC(Br)C1
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Safety Information

HS Code 
2933998090
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tert-butyl 3-bromoazetidine-1-carboxylate Usage And Synthesis

Synthesis

19540-05-7

24424-99-5

1064194-10-0

To a flame-dried 500 mL round-bottomed flask was added 1-amino-2,3-dibromopropane hydrobromide (17) (3.5 g, 11.8 mmol, 1 equiv.) and stirred solvent-free under argon protection to obtain a fine powder of 17 (or crystals of 17 were manually ground to a fine powder before use). Anhydrous THF (35 mL) was added to the flask and the mixture was cooled to -78°C. PhLi solution (1.8 M in dibutyl ether, 18.5 mL, 35.3 mmol, 3 eq.) was slowly added via syringe, and the reaction mixture was stirred for 2 hr at -78°C. Subsequently, MeCN (112 mL), LiBr (~42 g, 35.3 mmol, 3 eq.), and Boc2O (5.4 mL, 23.6 mmol, 2 eq.) were added to the reaction mixture, and the mixture was slowly warmed from -78°C to room temperature overnight. The reaction mixture was poured into water (200 mL) and washed sequentially with saturated aqueous NaHCO3, aqueous Na2S2O3 (50 mL), and then extracted with ether (3 x 150 mL). The organic layers were combined, washed with brine (50 mL), dried over Na2SO4 and concentrated. The crude product was purified by fast chromatography (silica gel, 5-20% EtOAc in hexane solution) to afford the target product tert-butyl 3-bromoazetidine-1-carboxylate (20) (2.21 g, 79%). Physical state: transparent liquid; Rf = 0.38 (1:9 EtOAc/hexane, KMnO4 color development); 1H NMR (500 MHz, CDCl3): δ 4.55-4.46 (m, 3H), 4.22-4.14 (m, 2H), 1.44 (s, 9H); 13C NMR (126 MHz, CDCl3): δ 155.8 , 80.2, 60.3 (br, 2C), 33.0, 28.4 (3C); all spectral data are in agreement with literature reports.

References

[1] Arkivoc, 2018, vol. 2018, # 4, p. 195 - 214

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