Home Cart Sign in  
Chemical Structure| 40167-10-0 Chemical Structure| 40167-10-0

Structure of 40167-10-0

Chemical Structure| 40167-10-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 40167-10-0 ]

CAS No. :40167-10-0
Formula : C15H14O2
M.W : 226.27
SMILES Code : O=CCC1=CC=C(OCC2=CC=CC=C2)C=C1
MDL No. :MFCD11553534

Safety of [ 40167-10-0 ]

Application In Synthesis of [ 40167-10-0 ]

* 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 [ 40167-10-0 ]

[ 40167-10-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 61439-59-6 ]
  • [ 40167-10-0 ]
YieldReaction ConditionsOperation in experiment
95% With 2-iodoxybenzoic acid; In dimethyl sulfoxide; at 25℃; for 3h; To a solution of compound 9 (7.0 g, 30.7 mmol) in DMSO (15 mL),IBX (12.9 g, 46mmol)was added and suspensionwas stirred for 3 h atroom temperature. TLC examination (EtOAc/hexane, 1:3) indicatedthe completion of the reaction. EtOAc (350 mL) was added to thereactionmixture. The insoluble solidswere filtered off under suction.The EtOAc layer was washed with water (3 150 mL), brine(1 150mL), and dried over anhydrous Na2SO4. The drying agent wasfiltered off and the solventwas evaporated under reduced pressure to afford the product,10 (6.6 g, 95%)was characterized by proton and 13CNMR. The proton NMR matched well with the one reported in literature.1HNMR (CDCl3) d 3.63 (d, 2H, J¼2.1Hz), 5.06 (s,2H), 6.98 (d, 2H,J¼8.4 Hz), 7.13 (d, 2H, J¼8.4 Hz), 7.30e7.60 (m, 5H), 9.72 (t, 1H,J¼2.1 Hz); 13C NMR d 49.7, 70.0, 115.3 (2C), 124.0, 127.5 (2C), 128.0,128.6 (2C),130.7 (2C),136.8,158.1,199.8 andMS(ESth)m/z 227 (MthH).
79% With Dess-Martin periodane; In dichloromethane; at 20℃; for 2h; [472] Step C: (4-benzyloxy-phenyl)-acetaldehyde [473] 2-(4-Benzyloxy-phenyl)-ethanol (0.64 g, 2.80 mmol) obtained in Step B wasdissolved in DCM (10 mL), and Dess-Martin periodinane (2.38 g, 5.60 mmol) wasadded thereto. The reactant was stirred at room temperature for 2 hours,diluted with DCM, and washed with Na2S2O3·5H2O aqueoussolution. The remained organic solution was dried with MgSO4 andconcentrated under reduced pressure. The residue was purified by columnchromatography (eluent, EtOAc/Hex = 1/5) to obtain the title compound (0.50 g,79%).[474] 1H NMR (400 MHz, CDCl3)delta 9.70(t, 1H), 7.44-7.29(m, 5H), 7.12(d, 2H), 6.97(d, 2H), 5.02(s, 2H),3.61(d, 2H)
79% With Dess-Martin periodane; In dichloromethane; at 0 - 20℃; for 3h; Into a 250-mL round-bottom flask, Dess-Martin periodinane (CAS 87413-090) (11.0 g, 1.20 equiv) was added into a solution of <strong>[61439-59-6]2-[4-(benzyloxy)phenyl]ethan-1-ol</strong> (5.0 g, 21.90 rnrriol, 1.00 equiv) in dichloromethane (100 mL) at 0 degrees. The reaction mixture was stirred for 3 h at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column eluting with ethyl acetate/petroleum ether (1 : 1). This resulted in 3.9 g (79%) of 2-[4-(benzyloxy)phenyl]acetaldehyde as a solid.
With Dess-Martin periodane; In dichloromethane; at 20℃; for 0.5h; Dess-Martin periodinane (1.103 g, 2.60 mmol) was added to a solution of <strong>[61439-59-6]2-(4-benzyloxyphenyl)ethanol</strong> (0.457 g, 2.00 mmol) in CH2Cl2 (15 mL) at room temperature, and the resultant mixture allowed to stir for 0.5 h. A 1:1 mixture of Na2S2O3 (1.5 M) and satd aq NaHCO3 (30 mL) was added and the mixture stirred until two clear layers formed. The organic phase was taken up in ether (20 mL), washed with water (3 × 20 mL) and brine (3 × 20 mL), dried (MgSO4), filtered and concentrated under reduced pressure to afford the crude aldehyde 5b as a clear yellow oil which was used in the subsequent step without purification.

 

Historical Records

Technical Information

Categories