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Chemical Structure| 87453-54-1 Chemical Structure| 87453-54-1

Structure of 87453-54-1

Chemical Structure| 87453-54-1

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Product Details of [ 87453-54-1 ]

CAS No. :87453-54-1
Formula : C8H14O
M.W : 126.20
SMILES Code : C=CC(C1CCCC1)O
MDL No. :MFCD00061051

Safety of [ 87453-54-1 ]

Application In Synthesis of [ 87453-54-1 ]

* 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 [ 87453-54-1 ]

[ 87453-54-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 50638-47-6 ]
  • [ 87453-54-1 ]
  • [ 625446-78-8 ]
YieldReaction ConditionsOperation in experiment
79% With sodium hydrogencarbonate;bis-triphenylphosphine-palladium(II) chloride; In 1-methyl-pyrrolidin-2-one; at 20 - 140℃; for 4h; To a magnetically stirring solution of <strong>[50638-47-6]4-bromo-2-chloroanisole</strong> (0.50 g, 2.61 mmol) and 1- CYCLOPENTYL-2-PROPEN-1-OL (1.5 eq, 0.49 g, 3.88 mmol) in anhydrous N-methylpyrrolidinone (3.0 mL), under argon at room temperature, was added sodium bicarbonate (1.2 eq, 0.26 g, 3.10 mmol) followed by DICHLOROBIS (TRIPHENYLPHOSPHINE) PALLADIUM (II) (0.02 eq, 36.7 mg, 0.05 MMOL). The resulting mixture was heated to 140 C in an oil bath and maintained for 4 hours. The resulting dark reaction mixture was cooled to room temperature and poured into water (50 mL) and extracted with EtOAc (2 X 25 mL). The organics were washed with water (50 mL) and brine (50 mL) then dried over NA2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (1% through 10% EtOAc in Hexanes) to yield the intermediate ketone as a slightly yellow oil (0.49 g, 79%).
79% With sodium hydrogencarbonate;bis-triphenylphosphine-palladium(II) chloride; In 1-methyl-pyrrolidin-2-one; at 20 - 140℃; for 4h; To a magnetically stirring solution of <strong>[50638-47-6]4-bromo-2-chloroanisole</strong> (0.50 g, 2.61 mmol) and 1-Cyclopentyl-2-propen-1-ol (1.5 eq, 0.49 g, 3.88 mmol) in anhydrous N-methylpyrrolidinone (3.0 mL), under argon at room temperature, was added sodium bicarbonate (1.2 eq, 0.26 g, 3.10 mmol) followed by dichlorobis (triphenylphosphine) palladium (II) (0.02 eq, 36.7 mg, 0.05 mmol). The resulting mixture was heated to 140 C. in an oil bath and maintained for 4 hours. The resulting dark reaction mixture was cooled to room temperature and poured into water (50 mL) and extracted with EtOAc (2×25 mL). The organics were washed with water (50 mL) and brine (50 mL) then dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (1% through 10% EtOAc in Hexanes) to yield the intermediate ketone as a slightly yellow oil (0.49 g, 79%).
  • 2
  • [ 33839-11-1 ]
  • [ 87453-54-1 ]
  • [ 749929-11-1 ]
YieldReaction ConditionsOperation in experiment
47% With sodium hydrogencarbonate;bis-triphenylphosphine-palladium(II) chloride; In 1-methyl-pyrrolidin-2-one; at 140℃; for 5h; A mixture of bromide (1.3g, 6. 02MMOL, from step 1), 1-CYCLOPENTYL-2-PROPEN-1-OL (1.14g, 9. 07mmot), DICHLOROBIS (TRIPHENYLPHOSPHINE) PALLADIUM (LL) (85 mg, 0 12 mmol), sodium bicarbonate (0.61 g, 7.25 MMOT) in N-METHYLPYRROLIDINONE (12mL) was heated to 140 C under N2 for 5h. The reaction mixture was partitioned between 1N HCl and EtOAc. The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated'to a brown oil. The oil was purifed by silica gel chromatography to give the title compound as a yellow oil (0.74g, 47%). 1H NMR (CDCL3): No. ?1. 17 (t, 3H, J = 7.6 Hz), 1. 54-1. 80 (M, 9H), 1.17 (q, 2H, J= 7. 6 HZJ,-2. 73 (m, 2H), 2.84 (m, 2H), 3.80 (s, 3H), 6.75 (d, 1H, J= 8. 0Hz), 6.97 (m, 2H).
 

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