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Chemical Structure| 5754-35-8 Chemical Structure| 5754-35-8

Structure of 5754-35-8

Chemical Structure| 5754-35-8

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Product Details of [ 5754-35-8 ]

CAS No. :5754-35-8
Formula : C5H11NO2
M.W : 117.15
SMILES Code : NCCC1OCCO1
MDL No. :MFCD00142756

Safety of [ 5754-35-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H226-H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:3(8)
UN#:2733
Packing Group:

Application In Synthesis of [ 5754-35-8 ]

* 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 [ 5754-35-8 ]

[ 5754-35-8 ] Synthesis Path-Downstream   1~35

  • 1
  • [ 5754-35-8 ]
  • [ 74-88-4 ]
  • (2-[1,3]dioxolan-2-yl-ethyl)-trimethyl-ammonium; iodide [ No CAS ]
  • 2
  • [ 64-17-5 ]
  • [ 185563-61-5 ]
  • [ 5754-35-8 ]
  • 4
  • [ 5754-35-8 ]
  • [ 50371-52-3 ]
  • [ 154468-43-6 ]
YieldReaction ConditionsOperation in experiment
In acetonitrile; 4,5-Dibromo-N-[2-(1,3-dioxolan-2-yl)ethyl]pyrrole-2-carboxamide (11). A solution of <strong>[5754-35-8]2-(2-aminoethyl)-1,3-dioxolane</strong> (2.4 g, 20.6 mmol) and 4,5-dibromopyrrol-2-yl trichloromethyl ketone (7.6 g, 20.5 mmol) in 30 mL of acetonitrile was stirred at room temperature for 16 h. The reaction mixture was filtered and the precipitate 11 (6.8 g, 90%) was collected as a colorless solid: mp 155-157 C.; 1H NMR (CDCl3) d 1.99 (dt, 2H, J=6.0, 4.2), 3.61 (dt, 2H, J=6.0, 5.6), 3.92 (m, 2H), 4.05 (m, 2H), 5.00 (t, 1H, J=4.2), 6.51 (d, 1H, J=2.8), 6.66 (bs, 1H), 10.57 (bs, 1H); 13C NMR (CD3COCD3) d 34.3 (e), 35.5 (e), 65.4*2 (e), 99.4 (e), 103.4 (o), 105.4 (e), 113.0 (o), 129.1 (e), 160.0 (e); IR (nujol) 3358, 1646, 1569, 1412, 1372 cm-1; UV (CH3OH) 1max 275, 233, 214 (sh) nm; MS m/z (relative intensity) 371 (M++5, 50), 369 (M++3, 100), 367 (M++1, 50), 289 (13), 118 (25), 101 (50), 73 (30); Anal. Calcd for C8H10N2O2Br2: C, 32.63; H, 3.29; N, 7.61; Found: C, 32.77; H, 3.17; N, 7.51.
  • 5
  • [ 5754-35-8 ]
  • [ 2969-81-5 ]
  • [ 111752-09-1 ]
  • 6
  • [ 5754-35-8 ]
  • [ 69367-52-8 ]
  • [ 104568-95-8 ]
  • 7
  • [ 5754-35-8 ]
  • [ 14527-26-5 ]
  • [ 82892-14-6 ]
  • 8
  • [ 5754-35-8 ]
  • [ 141-97-9 ]
  • (E)-3-(2-[1,3]Dioxolan-2-yl-ethylamino)-but-2-enoic acid ethyl ester [ No CAS ]
  • 9
  • [ 5754-35-8 ]
  • ethyl α-bromo-4-fluorobenzeneacetate [ No CAS ]
  • ethyl α-<<2-(1,3-dioxolan-2-yl)ethyl>amino>-4-fluorobenzeneacetate [ No CAS ]
  • 10
  • [ 5754-35-8 ]
  • [ 7152-15-0 ]
  • [ 135833-73-7 ]
  • 11
  • [ 5754-35-8 ]
  • [ 4949-44-4 ]
  • [ 135833-70-4 ]
  • 12
  • [ 82891-99-4 ]
  • [ 5754-35-8 ]
  • 15
  • [ 5754-35-8 ]
  • [ 1477-50-5 ]
  • N-[2-(1,3-dioxolan-2-yl)ethyl]-1H-indole-2-carboxamide [ No CAS ]
  • 16
  • [ 5754-35-8 ]
  • [ 167631-58-5 ]
  • N-[2-(1,3-dioxolan-2-yl)ethyl]-3-iodo-1H-indole-2-carboxamide [ No CAS ]
  • 17
  • [ 5754-35-8 ]
  • [ 30562-34-6 ]
  • 17-[2-(dioxolan-2-yl)ethyl]amino-17-demethoxygeldanamycin [ No CAS ]
  • 18
  • [ 5754-35-8 ]
  • [ 54644-12-1 ]
  • 5-ethoxy-2-phenyl-oxazole-4-carboxylic acid (2-[1,3]dioxolan-2-yl-ethyl)-amide [ No CAS ]
  • 19
  • [ 5754-35-8 ]
  • [ 463-71-8 ]
  • [ 1246860-85-4 ]
YieldReaction ConditionsOperation in experiment
100% With calcium carbonate; In dichloromethane; water; at 20℃; for 18.0833h; CaCO3 (1.36g, 13.66mmol) was added to a vigorously stirred solution of 2-[1 ,3]dioxolan- 2-yl-ethylamine (1.Og, 8.54mmol) in DCM (20ml) and water (10ml). Thiophosgene (0.85ml, 11.10mmol) was added dropwise over 5 min and the resultant biphasic mixture was vigorously stirred at RT for 18h. The reaction mixture was diluted with water (40ml) and the organic phase was separated. The aqueous layer was extracted with DCM (2 x 40ml) and the combined organic layers were washed with water (50ml) followed by brine (50ml), dried (Na2SO4) and concentrated in vacuo to give a yellow oil (1.36g, 100%). This material was used in the next step without further purification.
  • 20
  • [ 5754-35-8 ]
  • [ 474759-03-0 ]
  • 22
  • [ 5754-35-8 ]
  • [ 135833-79-3 ]
  • 23
  • [ 5754-35-8 ]
  • [ 110862-44-7 ]
  • 24
  • [ 5754-35-8 ]
  • [ 135833-80-6 ]
  • 25
  • [ 5754-35-8 ]
  • [ 104568-93-6 ]
  • 26
  • [ 5754-35-8 ]
  • [ 110862-43-6 ]
  • 27
  • [ 5754-35-8 ]
  • [ 104568-94-7 ]
  • 28
  • [ 5754-35-8 ]
  • [ 135833-89-5 ]
  • 29
  • [ 5754-35-8 ]
  • [ 135833-74-8 ]
  • 30
  • [ 5754-35-8 ]
  • [ 135833-71-5 ]
  • 31
  • [ 5754-35-8 ]
  • [ 104568-72-1 ]
  • 32
  • [ 5754-35-8 ]
  • 1-(2-[1,3]Dioxolan-2-yl-ethyl)-5-(4-fluoro-phenyl)-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester [ No CAS ]
  • 33
  • [ 5754-35-8 ]
  • [ 135833-76-0 ]
  • 34
  • [ 5754-35-8 ]
  • [ 135833-90-8 ]
  • 35
  • [ 5754-35-8 ]
  • [ 135833-91-9 ]
 

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