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Chemical Structure| 26066-15-9 Chemical Structure| 26066-15-9

Structure of 26066-15-9

Chemical Structure| 26066-15-9

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Product Details of [ 26066-15-9 ]

CAS No. :26066-15-9
Formula : C10H14O2
M.W : 166.22
SMILES Code : OCC1=CC=CC(OC(C)C)=C1
MDL No. :MFCD06201145

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Application In Synthesis of [ 26066-15-9 ]

* 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 [ 26066-15-9 ]

[ 26066-15-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75792-33-5 ]
  • [ 26066-15-9 ]
YieldReaction ConditionsOperation in experiment
To a solution of 3-Isopropoxy-benzaldehyde 14-1 (20 g, 122 mmol) in methanol (400 mL), sodium borohydride (5g) is added in several portions at 0 C. The resulting mixture is then stirred at rt for 3 h. The reaction is quenched by addition of saturated NH4OH. Extracted (EtOAc), concentrated, a colorless oil 14-2 (MH+, 166) is obtained and use without purification. Re- dissolve (3-Isopropoxy-phenyl)- methanol 14-2 in ether (244 mL) PBr3 (11.5 mL, 122 mmol) is added dropwise at 0 0C. The reaction mixture is stirred at 0 0C then rt for 3 h, quenched (MeOH), extracted (EtOAc), concentrated, a colorless oil 14-3 is obtained. (MH+, 288)
With sodium tetrahydroborate; In methanol; dichloromethane; at 0℃; Step 10b: Prep of 3-isopropoxybenzylalcohol; To a 1 molar solution of 3-isopropoxy benzaldehyde (102g, 0.621 moles) in methanol (620 mL) cooled to zero degrees was added (slowly) sodium borohydride powder (25.8g, 0.683 moles)-dissolved in a minimum of methylene chloride and passed through a plug of silica gel washing with more methylene chloride until the silica gel was free of the product. The eluent was stripped to an oil and pumped on high vacuum overnight. lH NMR (400 MHz, CDC13) δ 7.25 (m, IH), 6.9 (bs, 2H), 6.8 (db, J = 8 Hz, IH), 4.65 (d, J = 8Hz, 2H), 4.55 (pentet, J = 6 Hz, IH), 1.7 (m, IH), 1.34 (d, J = 6 Hz, 6H).LCMS ion fragment = appears as 367.2
36.32 g (95%) With sodium borohydrid; In ethanol; water; (b) To m-isopropoxybenzaldehyde (38 g, 0.23 mol) in 500 mL of ethanol was added slowly sodium borohydride (12.2 g, 0.32 mol) over a period of 1 h and the mixture was stirred for 2 h, filtered, and concentrated to 100 mL of its volume. The above mixture was diluted with 50 mL of water, neutralized with sulfuric acid solution with cooling, and was extracted with ether (4*100 mL). The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to afford 36.32 g (95%) of m-isopropoxybenzyl alcohol.
 

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