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Chemical Structure| 1311166-10-5 Chemical Structure| 1311166-10-5

Structure of 1311166-10-5

Chemical Structure| 1311166-10-5

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Product Details of [ 1311166-10-5 ]

CAS No. :1311166-10-5
Formula : C9H16O3
M.W : 172.22
SMILES Code : O=C(C1CC(O)C1)OC(C)(C)C
MDL No. :MFCD20257857

Safety of [ 1311166-10-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335-H227
Precautionary Statements:P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501

Application In Synthesis of [ 1311166-10-5 ]

* 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 [ 1311166-10-5 ]

[ 1311166-10-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 145549-76-4 ]
  • [ 1311166-10-5 ]
YieldReaction ConditionsOperation in experiment
Reference Example 5; Tert-butyl 3-azidecyclobutane carboxylate; Step 1:; To ethanol solution (2.9 L) comprising <strong>[145549-76-4]tert-butyl 3-oxocyclobutane carboxylate</strong> (490 g) obtained from Reference example 4, ethanol suspension (1.8 L) comprising sodium borohydride (54.4 g) was added while maintaining the temperature at 5° C. After stirring for one hour, the reaction solution was added with ammonium chloride solution to terminate the reaction. The mixture was extracted with dichloromethane and the organic layer was dried over magnesium sulfate. Solids were removed, and the filtrate was dried under reduced pressure.
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 5℃; for 2h; A mixture of tert-butyl 3- oxocyclobutanecarboxylate (15, 1.50 g, 8.8 mmol) in THF:MeOH (3 : 1 , 16 mL) was added dropwise to a stirring slurry of sodium borohydride (0.167 g, 4.4 mmol) in THF (8 mL) in round bottom flask cooled in an ice bath. The mixture was stirred at 0-5 °C for two hours. Water was added dropwise (10 mL) followed by aq. Na2C03, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over sodium sulfate. After filtration, the organic layer was concentrated to give the crude tert-butyl 3- hydroxycyclobutanecarboxylate (16) as a white semi-solid (2.3 g, 100percent), which was used in the next step without purification. p-Toluenesulphonyl chloride (4.201 g, 0.022 moles) was added to a stirring solution of crude tert-butyl 3 -hydroxycyclobutanecarboxylate (16, 2.30 g, 8.8 mmol) in dry pyridine (10 mL) and CH2C12 (20 mL) at 0 °C. The mixture was allowed to warm to room temperature and stirred under nitrogen overnight. The solvent was then removed under reduced pressure and the residue was partitioned between ethyl ether (100 mL) and 0.5 N aq. HC1 (20 mL). The organic layer was separated and washed with saturated NaHC03 and brine, and dried (Na2S04). After filtration, the solvent was removed under reduced pressure and the residue purified by silica gel flash chromatography (0-50percent EtOAc-hexane) to afford tert-butyl 3- (tosyloxy)cyclobutanecarboxylate (17) as a colorless oil that slowly solidified at room temperature (2.6 g, 90percent yield over 2 steps). 1H NMR (300 MHz, CDC13): delta 7.79 (d, 2H, J = 8.4 Hz), 7.35 (d, 2H, J = 8.1 Hz), 4.72 (m, 1H), 2.60-2.30 (m, 8H), 1.44 (s, 9H).
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 5℃; for 2h; A mixture of tert-butyl 3- oxocyclobutanecarboxylate (1, 1.50 g, 8.8 mmol) in THF:MeOH (3 : 1 , 16 mL) was added dropwise to a stirring slurry of sodium borohydride (0.167 g, 4.4 mmol) in THF (8 mL) in round bottom flask cooled in an ice bath. The mixture was stirred at 0-5 °Cfor two hours. Water was added dropwise (10 mL) followed by aq. Na2CO3, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over sodium sulfate.After filtration, the organic layer was concentrated to give the crude tert-butyl 3- hydroxycyclobutanecarboxylate (2) as a white semi-solid (2.3 g, 100percent),
 

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