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Chemical Structure| 926645-58-1 Chemical Structure| 926645-58-1

Structure of 926645-58-1

Chemical Structure| 926645-58-1

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Product Details of [ 926645-58-1 ]

CAS No. :926645-58-1
Formula : C15H24O3
M.W : 252.35
SMILES Code : CC1(C)[C@@H]2C[C@H]1C(O)C=C2COC(C(C)(C)C)=O

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Application In Synthesis of [ 926645-58-1 ]

* 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 [ 926645-58-1 ]

[ 926645-58-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 926645-58-1 ]
  • [ 56469-10-4 ]
  • [ 113449-78-8 ]
YieldReaction ConditionsOperation in experiment
With boron trifluoride diethyl etherate; In dichloromethane; at -15 - -10℃; for 7h; To a mixture of 1.1 molar equivalents of 5 and 1.0 molar equivalent of 12 in 24 volumes of methylene chloride were added four molar equivalents of boron trifluoride etherate, at (-15)-(-10) C. over one hour. The reaction mixture was maintained at the above temperature for 2.5 hours, then treated with another four molar equivalents of boron trifluoride etherate over one hour and stirred at the same temperature for another 2.5 hours. The reaction mixture was poured onto 0.5 parts of crushed ice containing 29 molar equivalents of sodium bicarbonate and left overnight at 20-25 C. The organic layer was separated and washed 3 times with 1.4 volumes (each) of 5% aqueous solution of sodium bicarbonate and dried over 0.05 parts of anhydrous sodium sulphate. The solvent was removed in vacuum at 50 Torr and 45 C. The residue was passed through 10 parts of silica gel 60-230 mesh using toluene as eluent. The fractions containing dexanabinol pivalate were collected and the solvent was removed in vacuum to afford dexanabinol pivalate (13) as an oil.
A 0.5 liter reactor previously filled with nitrogen, was charged with 25.25 g of 5 (0.1 mole) and 36.3 g of 12 (0.14 mole) in 247 ml of DCM. The reaction mixture was cooled to (-15)-(-20) C. under stirring and while keeping the temperature below -14 C. 42.6 g of boron trifluoride etherate were added. The resulting brownish solution was maintained at -15 C. for at least 1 hr. When the reaction was completed, a previously prepared solution of 15.15 g of sodium bicarbonate in 288 ml of water was added while letting the temperature rise up to 20 C. Then the two phases were separated. The organic phase was washed again with sodium bicarbonate solution and again phases were separated. To the organic phase 76 ml of water were added and then 40 g of sodium hydroxide 30.5% solution. After 10 minutes of stirring the two phases were separated. The organic phase was washed with 100 ml of water and again phases were separated. Then the organic phase was acidified with hydrochloric acid at 15-20 C. until pH 4-4.5 and the phases were separated. The organic phase was washed with 100 ml of water and then phases were separated. The solvent was removed under reduce pressure at 40-50 C. The oily residue was diluted with 150 ml of THF. The solution obtained was cooled to 20 C. The product (13) was not further isolated and it was used in the next step as a solution in THF.
With boron trifluoride diethyl etherate; In dichloromethane; at -11℃; for 0.5h;Inert atmosphere; (+)-4-hydroxymyrtenol pivalate (RTE.1.2C) (Lot2213- 170-3, 84.1%; 0.28 g, 0.86 mmoles, 1.0 equiv) was charged into a 40 mL scintillation vial with septum and nitrogen inlet. The vial was charged with dimethylbicyclo[3.1.1]hept-2-ene-2-methanol (DMHR) (260 mg, 1.2 equiv). Next the vial was charged with CH2CI2 (5 mL) and the suspension was cooled with an ice/salt bath. The reaction was then charged with BF3 etherate (0.42 mL, 3.5 equivs) added dropwise over 2 minutes by syringe. The resulting brown solution was then stirred cold for 30 mins (reaching a bath temperature of -11C). An aliquot was withdrawn and quenched in a small volume of water. After extracting with CH2CI2 progress was checked by TLC in 3 systems (all ethyl acetate/ heptane). There appeared to be no RTE.1.2C remaining. There was unreacted DMHR well separated from the new spot. The reaction was then quenched in the cold by gradual addition of water (5 mL, 5 volumes). The reaction was allowed to warm with vigorous stirring. The layers were separated by pipet and the bottom layer (CH2CI2, product) was set aside. The aqueous layer was then extracted lx with CH2CI2 (5 mL, 5 volumes.) The combined organic layers were then washed with saturated sodium bicarbonate (5 mL, 5 volumes.) Next the organic layers were washed with 25% sodium hydroxide (0.5 mL). After separating these layers the organic layers were adjusted to pH of ~1 with dropwise addition of 1 N HC1. Then the layers were washed 2x with water (5 mL). The organic layers then concentrated (Rotovap, 30 -40C). The crude product was taken up in CH2CI2 and a few drops of methanol and transferred to a silica flash column. Elution with starting at 0-10% ethyl acetate/heptane gave elution of product well separated from DMHR and partially from two spots just above and below the major. Fractions containing the product spot were concentrated (Rotovap, 50C). The material was transferred to a tared vial and residual solvents were chased with portions of LC- 2213-172-1 Major peak 33.983 mins (75.25%) plus minor peak 35.125 mins (15.98%). LC-MS- 2213-172-2 Major peak 9.420 mins (88.69% at 210 nm, ES" 413 loss of t-butyl). NMR (CDC )- 2213-172-1 1H supports desired structure with good apparent purity. Potency determination by wt/wt (1,4-dimethoxybenzene) as 2213-172-4 A&B gave average of 77.7%. Yield 0.26 g or calculated 50% from potency data (Lot2213-172-3).
 

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