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Chemical Structure| 45804-94-2 Chemical Structure| 45804-94-2

Structure of 45804-94-2

Chemical Structure| 45804-94-2

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Product Details of [ 45804-94-2 ]

CAS No. :45804-94-2
Formula : C9H10O
M.W : 134.18
SMILES Code : OCC1=CC=CC(C=C)=C1

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Application In Synthesis of [ 45804-94-2 ]

* 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 [ 45804-94-2 ]

[ 45804-94-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19955-99-8 ]
  • [ 45804-94-2 ]
YieldReaction ConditionsOperation in experiment
99% With formic acid; iron(II) tetrafluoroborate hexahydrate; tris(2-diphenylphosphinoethyl)phosphine; In tetrahydrofuran; at 60℃; for 2h;Schlenk technique; Inert atmosphere; General procedure: Fe(BF4)2·6H2O (0.7 mg; 0.002 mmol) and tris[2-(diphenyl-phosphino)-ethyl]phosphine [P(CH2CH2PPh2)3; tetraphos] (1.4 mg; 0.002 mmol) are placed in a Schlenk-tube under argon atmosphere. 1 mL dry tetrahydrofurane is added and the purple solution is stirred for 2 min. Cinnamaldehyde (63 μL; 0.5 mmol) and 100 μL n-hexadecane as an internal GC-standard are injected and a sample is taken for GC-analysis. The solution is heated to 60 C and the reaction starts by addition of 1.1 equiv formic acid (22 μL; 0.55 mmol). After 2 h, a second sample is taken for GC-analysis and conversion and yield are determined by comparison with authentic samples. For the isolation, the reaction is scaled up by a factor of 20. When the reaction is completed, the reaction solution is diluted with a mixture of n-hexane and ethyl acetate (3:1), filtered through a plug of silica and the solvent removed in vacuum.
99% With methanol; at 22℃; for 1h;Inert atmosphere; NaBH4 (327 mg, 8.66 mmol) was slowly added to a solution of 3- vinylbenzaldehyde (1.00 mL, 7.87 mmol) in MeOH (20 mL) at 22 C under N2. The mixture was stirred at 22 C for 1 h and concentrated under reduced pressure. The residue was purified by S1O2 chromatography (EA/ hexanes) to provide 1.05 g (99 %) of (3-vinylphenyl) methanol (INT 59-1). LCMS-ESI (m/z) mass not observed, tR = 2.00 min (Method 13). NMR (400 MHz, CDCh) d 7.42 (s, 1H), 7.37 - 7.30 (m, 2H), 7.26 (d, J = 3.1 Hz, 1H), 6.73 (dd, J = 17.6, 10.9 Hz, 1H), 5.78 (dd, J = 17.6, 0.9 Hz, 1H), 5.27 (dd, J = 10.9, 0.9 Hz, 1H), 4.70 (s, 2H), 1.67 (s, 1H).
 

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