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Chemical Structure| 171596-62-6 Chemical Structure| 171596-62-6

Structure of 171596-62-6

Chemical Structure| 171596-62-6

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Product Details of [ 171596-62-6 ]

CAS No. :171596-62-6
Formula : C13H14O3
M.W : 218.25
SMILES Code : CC(C1=CC([C@]2([H])[C@](O2)([H])C(C)(C)O3)=C3C=C1)=O

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Application In Synthesis of [ 171596-62-6 ]

* 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 [ 171596-62-6 ]

[ 171596-62-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 19013-07-1 ]
  • [ 171596-62-6 ]
  • [ 178458-56-5 ]
  • 2
  • [ 19013-07-1 ]
  • [ 171596-62-6 ]
YieldReaction ConditionsOperation in experiment
92% With sodium hydroxide; sodium hypochlorite; sodium dihydrogenphosphate;(R)-1-phenyl-1,2-bis(3,5-di-tert-butyl-salicylideamino)ethane-manganese (III) chloride; In dichloromethane; water; at 20℃;pH 11.3; A solution of sodium hypochlorite (8.6ml, 17.3%w/v), water (14ml) and Na2HPO4 (0.05M, 10ml) was adjusted to pH 11.3 with 8N NaOH. 6-Acetyl-2,2-dimethyl chromene (2g) and E14 (65.6 mg 1mol %) and dichloromethane (20ml) was added and the mixture stirred rapidly at room temperature overnight. The mixture was diluted with dichloromethane (50ml) and filtered through celite. The two layers were separated and the organic phase washed with water (100ml) the evaporated to dryness to give the title compound (2.0g 92%), ee = 67% by chiral HPLC.
60% With pyridine N-oxide; sodium hydroxide; sodium hypochlorite; sodium dihydrogenphosphate;(R,R)-[1,2-bis(3,5-di-tert-butylsalicylideamino)cyclohexane]manganese (III) chloride; In dichloromethane; water; for 1h;pH 11.0; A solution of sodium hypochlorite (54ml, 13.7% w/v), 0.05M NaHPO4 (50ml) and water (70 ml) were adjusted to pH 11.3 with 8N NaOH. 6-Acetyl-2,2-dimethyl chromene (10g 0.049 mol) and R,R-[1,2-bis (3,5-di-tert-butylsalicylideamino)cyclohexane]manganese (III) chloride catalyst (320mg 1 mol%), pyridine N-oxide (9.5g, 2eq) and dichloromethane (50ml) were mixed together and the mixture was stirred for 1 hour. The solution was diluted with DCM (200ml) and filtered through celite and the layers separated. The aqueous layer was re-extracted with DCM (200ml) then the organic layers combined. The organic phase was washed with water (2 x 400ml) and evaporated to dryness to give a brown oil 12g, ee 95% (chiral hplc). The oil was crystallised from IPE (2½ volumes) seeded with epoxide to give the title compound as an off-white/brown solid (6.45g, 60%) ee>99%.
44% With pyridine N-oxide; sodium hydroxide; sodium hypochlorite; sodium dihydrogenphosphate;(3S,4S)-bis-(3,5-di-tert-butylsalicylideamino)tetrahydrofuran-manganese (III) chloride; In dichloromethane; water; at 20℃; for 2h;pH 13.0; Sodium hypochlorite (21.5 ml, 17.3% w/v), water (34 ml) and 0.05M Na2HPO4 (25 ml) were adjusted to pH 13 with 8N NaOH. 6-Acetyl-2,2-dimethyl-2H-1-benzopyran (5.0g, 25 mmoles), pyridine N-oxide (5.0g, 52 mmoles) and the S,S-Mn Salen catalyst (3S,4S)-bis-(3,5-di-tert-butylsalicylideamino)tetrahydrofuranmanganese (III) chloride (D34, 152 mg, 1 mole %) were added with dichloromethane (50 ml) and the mixture stirred at room temperature. After 2 hrs the reaction was complete according to HPLC analysis. The mixture was diluted with dichloromethane and filtered through celite. The two phases were separated and the organic phase washed with water (200 ml), then evaporated to dryness under reduced pressure to give the crude title compound as a brown oil (5.0g). This was shown by chiral HPLC to have an e.e. of 94%. The title compound was obtained enantiomercially pure (e.e. >99.8%) by recrystallization of the crude product from diisopropyl ether in a recovery of 44%.
 

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