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Chemical Structure| 2396-61-4 Chemical Structure| 2396-61-4

Structure of 3,3'-Oxybis(propan-1-ol)
CAS No.: 2396-61-4

Chemical Structure| 2396-61-4

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Product Details of [ 2396-61-4 ]

CAS No. :2396-61-4
Formula : C6H14O3
M.W : 134.17
SMILES Code : OCCCOCCCO
MDL No. :MFCD00051023
InChI Key :SZXQTJUDPRGNJN-UHFFFAOYSA-N
Pubchem ID :32857

Safety of [ 2396-61-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 2396-61-4 ]

* 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 [ 2396-61-4 ]

[ 2396-61-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2396-61-4 ]
  • [ 58929-72-9 ]
YieldReaction ConditionsOperation in experiment
55% With phosphorus tribromide; at 20℃;Heating / reflux;Product distribution / selectivity; 6.2 EXAMPLES OF ILLUSTRATIVE COMPOUNDS OF THE INVENTION; Bis (3-bromopropyl) ether (104).; Under N2-atmosphere, phosphorus tribromide (7.2 mL, 20.5 g, 75.8 mmol) was added dropwise over 1 h to 103 (Buchanan, G. W. et al. Can. J Chem. 2000, 78, 316-321) (10.14 g, 75.6 mmol), causing self-heating to reflux. The reaction mixture was stirred overnight at room temperature, then distilled in vacuo to give an oil. This oil was dissolved in CH2C12 (100 mL), washed with water (100 mL), dried over Na2SO4, and concentrated in vacuo, affording 104 (10.9 g, 55 %) as a clear, colorless oil. Bp 68-70 C/0. 2 mmHg. 1H NMR (CDC13) : No. 3.56 (t, 4 H, J= 5.8), 3.51 (t, 4 H, J= 6.4), 2.10 (m, 4 H). 13C NMR (CDC13 = 77. 00 ppm) : 6 68. 17,32. 68,30. 59.
34% With phosphorus tribromide; at 20 - 90℃; To a flask containing compound 2 (11 g, 82.0 mmol), PBr3 (55 mL) was added slowly drop wise and the mixture stirred for 0.5 hours at ambient temperature followed by heating to 900C. After being stirred for 3 hours at this temperature the reaction mixture was quenched with ice (500 g) slowly, stirred continuously for 10 minutes and extracted with CH2Cl2 (2 X 700 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give compound 3 as a pale yellow liquid (7.24 g). Yield: 34%. 1HNMR (400 MHz, CDCl3): δ (ppm): 3.70-3.55 (t, 4H), 3.60-3.35 (t, 4H), 2.15-1.95 (m, 4H).
 

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