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Chemical Structure| 45347-82-8 Chemical Structure| 45347-82-8

Structure of 45347-82-8

Chemical Structure| 45347-82-8

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Product Details of [ 45347-82-8 ]

CAS No. :45347-82-8
Formula : C3H7NO
M.W : 73.09
SMILES Code : OC1CNC1
MDL No. :MFCD03695446
InChI Key :GMWFCJXSQQHBPI-UHFFFAOYSA-N
Pubchem ID :1514290

Safety of [ 45347-82-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:3259
Packing Group:

Application In Synthesis of [ 45347-82-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 45347-82-8 ]

[ 45347-82-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 45347-82-8 ]
  • [ 93107-30-3 ]
  • 1-cyclopropyl-6-fluoro-1,4-dihydro-7-[3'-hydroxy-1'-azetidinyl]-4-oxo-3-quinolinecarboxylic acid [ No CAS ]
  • 2
  • [ 45347-82-8 ]
  • [ 75-36-5 ]
  • [ 118972-96-6 ]
YieldReaction ConditionsOperation in experiment
14% With triethylamine; In tetrahydrofuran; at -78 - 30℃; for 3.16667h; Step 1-Synthesis of 1-(3-hydroxyazetidin-1-yl)ethan-1-one To a solution of azetidin-3-ol (3.0 g, 27.40 mmol) and triethylamine (8.33 g, 82.48 mmol) in tetrahydrofuran (150 mL) was added acetyl chloride (2.15 g, 27.39 mmol) dropwise with stirring at -78 C. over 10 min. The resulting solution was stirred for 3 h at 20-30 C. The solid material was removed by filtration. The filtrate was concentrated under vacuum and purified on a silica gel column (methanol/ethyl acetate (1/10)) to afford 500 mg (14%) of 1-(3-hydroxyazetidin-1-yl)ethan-1-one as yellow oil. 1H NMR (400 MHz, DMSO) delta 3.60 (t, J=4.8 Hz, 2H), 2.83 (t, J=4.8 Hz, 2H), 2.21 (s, 3H).
With triethylamine; In tetrahydrofuran; PREPARATION 8 1-Acetyl-3-azetidinol Acetyl chloride (923.1 g, 296 mmol) was added slowly to a stirring slurry of azetidin-3-ol (18.0 g, 246 mmol) and triethylamine (37.3 g, 369 mmol) in tetrahydrofuran (500 mL) maintained at -78 C. The reaction was allowed to warm slowly to ambient temperature over 2 h. The reaction mixture was filtered to remove some solid material and the solid was washed with tetrahydrofuran (~200 mL). The filtrate was concentrated in vacuo. The residue was diluted with hexane and concentrated (repeated twice) to give 23.2 g (82%) of a white solid. A small sample (0.5 g) was recrystallized from ethyl acetate and hexane to give 0.48 g of white solid, mp 57-60 C. Analysis: Calculated for C5 H9 NO2: C, 52.16; H, 7.88; N, 12.17. Found: C, 52.01; H, 7.94; N, 12.17.
  • 3
  • [ 61929-24-6 ]
  • [ 45347-82-8 ]
  • 1-(1,3,4-thiadiazol-2-yl)azetidin-3-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With racemic-2-(di-tert-butylphosphino)-1,1?-binaphthyl; tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; The requisite 1 -(1 ,3,4-thiadiazol-2-yl)azetidin-3-ol was synthesized from azetidin-3-ol and 2-bromo-1 ,3,4-thiadiazole in the presence of (0938) tn's(dibenzylideneacetone)dipalladium(0), 1 ,1 '-binaphthalen-2-yl(di-fe/f-butyl)phosphane (TrixiePhos), and cesium carbonate.
 

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[ 45347-82-8 ]

Chemical Structure| 18621-18-6

A102357 [18621-18-6]

Azetidin-3-ol hydrochloride

Reason: Free-salt