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Chemical Structure| 1187933-07-8 Chemical Structure| 1187933-07-8

Structure of 1187933-07-8

Chemical Structure| 1187933-07-8

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Product Details of [ 1187933-07-8 ]

CAS No. :1187933-07-8
Formula : C8H14O3
M.W : 158.20
SMILES Code : O=C(C1CC(O)CC1)OCC
MDL No. :MFCD12913653

Safety of [ 1187933-07-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1187933-07-8 ]

* 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 [ 1187933-07-8 ]

[ 1187933-07-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5400-79-3 ]
  • [ 1187933-07-8 ]
YieldReaction ConditionsOperation in experiment
To a 0 C solution of ethyl-3-oxo-cyclopentane-l- carboxylate (2.0 g) in THF (50 mL) was added NaBH4 (970 mg). The reaction mixture was maintained at 0 C for 30 min, and then overnight at ambient temperature. The reaction was then treated with H20 and diluted with Et20. The resulting layers were separated, and the aqueous layer was further extracted with Et20. The combined organic layers were washed with brine, dried over Na2S04, filtered and concentrated. The resulting crude product (a mixture of cis/trans isomers) was used in the next step without further purification.
With sodium tetrahydroborate; ethanol; at 20℃; Preparation No.39: 3-Hydroxy-cyclopentanecarboxylic acid ethyl ester; A solution of <strong>[5400-79-3]ethyl 3-oxocyclopentanecarboxylate</strong> (2.00 g, 12.81 mmol) in EtOH (20 mL) was treated with sodium borohydride (0.451 mL, 12.81 mmol) portionwise at RT (RT water bath to control exotherm) and the reaction was stirred overnight. The reaction was quenched with 2N HC1 to about pH=2 and extracted with CH2CI2, washed with water, dried over sodium sulfate, filtered and concentrated to oil. The crude product was further purified on silica gel using a gradient of 20-40% ethyl acetate in heptane. Pure product fractions and concentrate were combined to constant weight. NMR indicates an approximately 3:7 ratio of isomers. .H NMR (400 MHz, DMSO-d6) delta ppm 4.52-4.50 (m, 1H), 4.19-4.15 (m, 0.3H), 4.08-4.02 (m, 2.7H), 2.94-2.86 (m, 0.3H), 2.74-2.66 (m, 0.7H), 2.08-1.46 (m, 6H), 1.19-1.15 (m, 3H).
 

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