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Chemical Structure| 7116-48-5 Chemical Structure| 7116-48-5

Structure of 7116-48-5

Chemical Structure| 7116-48-5

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Product Details of [ 7116-48-5 ]

CAS No. :7116-48-5
Formula : C12H14O4
M.W : 222.24
SMILES Code : O=C(OCC)CCC1=CC=C2OCOC2=C1
MDL No. :MFCD09028865

Safety of [ 7116-48-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 7116-48-5 ]

* 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 [ 7116-48-5 ]

[ 7116-48-5 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 7116-48-5 ]
  • [ 2815-95-4 ]
YieldReaction ConditionsOperation in experiment
100% With sodium hydroxide; In water; at 20℃; for 2h; 72b (14.3 g, 66.3 mmol) and NaOH (10% w/w, 10 ml) were dissolved in methanol (100 mL) and stirred at room temperature for 2 hours. The solution was washed with EtOAc (2×100 mL) and the organic layer was partitioned from the aqueous layer. The aqueous layer was acidified to pH=5, extracted with EtOAc (2×100 mL), and dried over Na2SO4. The organic layer was concentrated down under vacuo to yield 13.2 g (100%) of compound 72c, which was used without further purification.
94% With water; sodium hydroxide; In methanol; for 2.5h;Inert atmosphere; To a stirred solution of 23 (6.92 g, 31.4 mmol) in ethylacetate (30 mL) was added 10% palladium on activated carbon (0.69 g, 10% w/w). The solution wasflushed with an atmosphere of hydrogen and stirred for 1 h. The reaction mixture was then filteredthrough a plug of celite and washed with ethyl acetate, solvent was then removed in vacuo to givesaturated ester 26 (6.9 g, 99%) which was then used without further purification.To a stirred solution of ester 26 (6.74 g, 30.0 mmol) in methanol (30 mL) was added aqueous NaOH(121 mL, 1M, 4 eq.) and stirred for 2.5 h. The mixture was then extracted with ethyl acetate (10 mL)and the aqueous layer acidified with aqueous 2M HCl. The aqueous phase was then extracted withethyl acetate (3 × 50 mL), dried (MgSO4) and solvent removed in vacuo to give the title compound 30(5.5 g, 94%) as a white solid. Rf = 0.44 (2:1 hexanes, ethyl acetate). Melting point: 80-82C. δH (400MHz; CDCl3) 2.64 (2H, t, J = 7.7 Hz, 2-H), 2.88 (2H, t, J = 7.7 Hz, 3-H), 5.93 (2H, s, -OCH2O-), 6.66 (1H,dd, J = 7.9, 1.4 Hz, 6′-H), 6.70 (1H, d, J = 1.4 Hz, 2′-H), 6.74 (1H, d, J = 7.9 Hz, 5′-H). δC (100 MHz; CDCl3)30.5 (C-2), 36.1 (C-3), 101.0 (-OCH2O-), 108.4 (C-2′), 108.9 (C-5′), 121.2 (C-6′), 134.1 (C-1′), 146.2 (C-3′),147.8 (C-4′), 179.1 (C-1). Values are in agreement with literature data [47].
 

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