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Chemical Structure| 76140-13-1 Chemical Structure| 76140-13-1

Structure of 76140-13-1

Chemical Structure| 76140-13-1

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Product Details of [ 76140-13-1 ]

CAS No. :76140-13-1
Formula : C7H9IO2
M.W : 252.05
SMILES Code : O=C1OC2C(I)CCC1C2
MDL No. :MFCD00604194

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Application In Synthesis of [ 76140-13-1 ]

* 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 [ 76140-13-1 ]

[ 76140-13-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 76140-13-1 ]
  • [ 4720-83-6 ]
YieldReaction ConditionsOperation in experiment
66% With 1,8-diazabicyclo[5.4.0]undec-7-ene; In benzene; for 6h;Heating / reflux; To 4-iodo-6-oxabicyclo [3.2. 1] octan-7-one (8.00 g, 31.7 mmol) in benzene (100 ml) was added 1, 8-diazabicyclo [5.4. 0] undec-7-ene (7.9 g, 32 mmol) under nitrogen, and the mixture was heated under reflux for 6 h. The white precipitate was filtered off from the cooled solution and washed with ether (100 ml). The combined filtrates were washed with water (50 ml), 1N HC1 (50 ml), and brine (25 ml), and then dried over magnesium sulfate. The solvents were removed by rotary evaporation to afford the alkene as a light brown oil (2.6 g, 66%)
58 g With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran;Reflux; To a solution of compound 2 (119g) in THF (1600ml) was added DBU (119ml) with stirring at room temperature, and the reaction mixture was gently refiuxed overnight with stirring. Some precipitate formed and TLC showed no starting material left. Reaction mixture was concentrated to dryness and dissolved in EtOAc (300ml), washed with 0.5M HC1 (200ml) until pH 2-3 of the aqueous layer and 0 (200ml). Aqueous layers were combined and were extracted with EtOAc (3x200rnl). Combined organic layers (900ml) were washed with brine, dried (Na2SQ4), filtered and concentrated to dryness to give compound 3 (58g). Purity: >95% by TLC
58 g With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran;Reflux; To a solution of compound 2 ( 1 19 g) in THF ( 1600 mL) was added DBU ( 1 19 mL) with stirring at room temperature and the reaction mixture was gently refluxed overnight with stirring. Some precipitate forms and TLC showed no starting material left. The reaction mixture was concentrated to dryness and dissolved in EtOAc (300 mL)mL), washed with 0.5 M HCI (200 mL)mL) until pH 2-3 of the aqueous wash, and then the organic layer was further washed with H20 (200 mL)mL). Aqueous layers were combined and extracted with EtOAc (3x200 mL)mL) to produce a second organic layer. Combined organic layers (900 mL)mL) were washed with brine, dried (Na2SC>4), filtered and concentrated to dryness to give compound 3 (58 g). Purity: >95% by TLC.
 

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