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Chemical Structure| 24393-59-7

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Product Details of [ 24393-59-7 ]

CAS No. :24393-59-7
Formula : C11H11NO4
M.W : 221.21
SMILES Code : O=C(OCC)/C=C/C1=CC=CC=C1[N+]([O-])=O
MDL No. :MFCD00956801
Boiling Point : No data available
InChI Key :TYYXOWPEFVCPDV-BQYQJAHWSA-N
Pubchem ID :5355496

Safety of [ 24393-59-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 24393-59-7 ]

* 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 [ 24393-59-7 ]

[ 24393-59-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24393-59-7 ]
  • [ 15121-84-3 ]
YieldReaction ConditionsOperation in experiment
85% With sodium tetrahydroborate; cobalt(II) chloride hexahydrate; ethanol; diisopropylamine; at 25 - 50℃; for 24h; Example 26: 2-(2-Nitrophenyl)ethanol (8a) To a stirred solution of ester 9 ((E)-ethyl 3-(2-nitrophenyl)acrylate)(7.0 g, 31 .7 mmol), C0CI2 6H2O (377 mg, 5 mol percent) and diisopropyl amine (320 mg, 10 mol percent) in 95percent ethanol (100 mL) was added NaBH4 (4.8 g, 126.8 mmol) slowly at 25 °C. It was then stirred for 24 h at 50 °C . After completion of the reaction (monitored by TLC), it was quenched with addition of water (20 mL) and ethyl ac etate (100 mL). The organic layer was separated and the aqueous layer extracted with ethyl acetate (2 x 50 mL). The combined organic layers were washed with brine (2 x 20 mL), dried over anhydrous Na2S04 and concentrated under reduced pressure to give the crude product. Chromatographic purification of crude product with petroleum ether/ethyl acetate (7:3 v/v) afforded alcohol 8a (5.74 g) as gum. Yield: 85percent; IR (CHCl3): umax 857, 968, 1029, 1060, 1245, 1440, 1507, 3430 cm"1; 1H NMR (200 MHz, CDCI3): delta 1 .85-1 .99 (m, 2H), 2.14 (br s, 1 H), 2.98 (t, J = 7.6 Hz, 2H), 3.70 (t, J = 6.2 Hz, 2H), 7.31 -7.55 (m, 3H), 7.86 (d, J = 7.7 Hz, 1 H); 13C NMR (50 MHz, CDCI3) : delta 29.1 , 33.2, 61 .6, 124.4, 126.8, 131 .8, 132.8, 136.7, 149.1 ; Anai. Laica Tor L9nn 03 requires C, 59.66; H, 6.12; N, 7.73; found C, 59.71 ; H, 6.15; N, 7.79percent.
85% With sodium tetrahydroborate; cobalt(II) chloride hexahydrate; diisopropylamine; In ethanol; at 25 - 50℃; for 24h; To a stirred solution of ester 9 ((E)-ethyl 3-(2-nitrophenyl)acrylate) (7.0 g, 31.7 mmol), CoCl2.6H2O (377 mg, 5 mol percent) and diisopropyl amine (320 mg, 10 mol percent) in 95percent ethanol (100 mL) was added NaBH4 (4.8 g, 126.8 mmol) slowly at 25° C. It was then stirred for 24 h at 50° C. After completion of the reaction (monitored by TLC), it was quenched with addition of water (20 mL) and ethyl acetate (100 mL). The organic layer was separated and the aqueous layer extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (2×20 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the crude product. Chromatographic purification of crude product with petroleum etherethyl acetate (7:3 vv) afforded alcohol 8a (5.74 g) as gum. [0083] Yield: 85percent; IR (CHCl3): umax 857, 968, 1029, 1060, 1245, 1440, 1507, 3430 cm?1; 1H NMR (200 MHz, CDCl3): delta 1.85-1.99 (m, 2H), 2.14 (br s, 1H), 2.98 (t, J=7.6 Hz, 2H), 3.70 (t, J=6.2 Hz, 2H), 7.31-7.55 (m, 3H), 7.86 (d, J=7.7 Hz, 1H); 13C NMR (50 MHz, CDCl3): delta 29.1, 33.2, 61.6, 124.4, 126.8, 131.8, 132.8, 136.7, 149.1; Anal. Calcd for C9H11NO3 requires C, 59.66; H, 6.12; N, 7.73. found C, 59.71; H, 6.15; N, 7.79percent.
 

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