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Chemical Structure| 53597-69-6 Chemical Structure| 53597-69-6

Structure of 53597-69-6

Chemical Structure| 53597-69-6

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Product Details of [ 53597-69-6 ]

CAS No. :53597-69-6
Formula : C6H12N3P
M.W : 157.15
SMILES Code : N12CN3CN(C2)CP(C3)C1
MDL No. :MFCD00154905
InChI Key :FXXRPTKTLVHPAR-UHFFFAOYSA-N
Pubchem ID :143061

Safety of [ 53597-69-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H228-H314-H401
Precautionary Statements:P210-P240-P241-P261-P272-P273-P280-P302+P352-P333+P313-P370+P378-P501
Class:4.1(8)
UN#:2925
Packing Group:

Application In Synthesis of [ 53597-69-6 ]

* 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 [ 53597-69-6 ]

[ 53597-69-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1633-83-6 ]
  • [ 53597-69-6 ]
  • [ 1430837-91-4 ]
YieldReaction ConditionsOperation in experiment
86.8% at 25.0℃; for 20.0h;Inert atmosphere; Schlenk technique; 0.300 g (1.9 mmol) of PTA were mixed with 780 μL (7.6 mmol, 4 eq) of 1,4-butanesultone for 20 h without any solvent. 5 mL of ether were then added and the white solid product was separated by filtration and washed with ether (0.483 g, 1.65 mmol, 86.8%). Solubility in water (25 C): 504 mg/mL. Data for 2 were as follows: 1H NMR (300 MHz, D2O, 25 C): δ 1.63 (m, 2H, CH2CH2SO3-), δ 1.80 (m, 2H, CH2CH2SO3-), δ 2.82 (m, 4H, CH2CH2CH2N+), δ 3.80 (m, 4H, PCH2N), δ 4.22 (s, 1H, PCH2N+), δ 4.23 (s, 1H, PCH2N+), δ 4.38 (d, 2JHH = 14 Hz, 1H, NCH2N), δ 4.52 (d, 2JHH = 14 Hz, 1H, NCH2N), δ 4.72 (d, 2JHH = 11 Hz, 2H, NCH2N+), δ 4.90 (d, 2JHH = 11 Hz, 2H, NCH2N+). 13C{1H}NMR (75.43 MHz, D2O, 25 C): δ 18.1 (s CH2SO3-), δ 21.2 (s, CH2CH2CH2SO3-), δ 30.1 (s, CH2CH2CH2N+), δ 45.2 (d, 1JPC = 21.4 Hz, PCH2N), δ 50.4 (s, CH2CH2CH2N+), δ 52.9 (d, 1JPC = 34 Hz, PCH2N+), δ 62.2 (s, CH2CH2N+), δ 69.4 (s, NCH2N), δ 78.8 (s, NCH2N+). 31P{1H} NMR (121.5 MHz, D2O, 25 C): δ -82.86 ppm (s). Anal. Calc. for C10H20N3O3PS (293): C, 40.94; H, 6.88; N, 14.33; S, 10.91. Found: C, 41.03; H, 6.97; N, 14.25; S, 10.82%. Electrospray MS (in H2O): observed m/z (M+H+) 294, (M+Na+) 316, calcd 294 for C10H21N3O3PS (MH+).
75% In acetone; at 60.0℃; for 24.0h;Inert atmosphere; An oven-dried 250 mL three-necked round-bottomed flask equipped with an additional funnel, a thermo-pocket, and a magnetic stir bar was evacuated and flushed with N2 three times. To this flask were added PTA (1.0 g, 1.0 equiv) and acetone (40 mL) under N2 atmosphere. The resulting mixture was stirred for 15 min at r.t. to obtain an almost clear solution. Next, 1,4-butanesultone (1.95 mL, 3.0 equiv) was added dropwise under N2 atmosphere. The reaction mixture was heated for 24 h at 60 C while stirring with a cooling condenser assembly. The mixture was cooled to r.t. and the solvent removed using cannula. The solid product was washed with acetone (3 10 mL) furnishing 1.4 g (75%) of PTABS as a white solid; mp 252-254 C (Lit.34 mp 252-255 C). IR (ATR): 3423, 3019, 2959, 1675, 1471, 1266, 1171, 1128, 1036, 991, 943, 922, 784, 652, 600 cm-1. 1H NMR (500 MHz, D2O): = 4.93 (d, J = 11.7 Hz, 2 H), 4.75 (d, J = 11.7 Hz, 2 H), 4.55 (d, J = 13.7 Hz, 1H), 4.39 (d, J = 13.7 Hz, 1H), 4.28 (d, J = 5.7 Hz, 2 H), 3.91 (t, J = 13.9 Hz, 2 H), 3.80 (dd, J = 14.9, 8.9 Hz, 2 H), 2.91 (dd, J = 17.4, 10.3 Hz, 4 H), 1.86 (dt, J = 16.0, 7.9 Hz, 2 H), 1.72 (dt, J = 14.7, 7.4 Hz, 2 H). 13C NMR{1H} (126 MHz, D2O): = 79.0, 69.5, 62.3, 53.2, 52.9, 49.9, 45.8, 45.7 (d, J = 20.9 Hz), 21.3, 18.2. 31P NMR (162 MHz, D2O): = -84.51. Anal. Calcd for C10H22N3O4PS (PTABS*H2O): C, 38.58; H, 7.12; N, 13.50; S, 10.30. Found: C, 38.87; H, 6.86; N, 13.52; S, 9.96.
 

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