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176251-49-3

176251-49-3 Structure

176251-49-3 Structure
IdentificationBack Directory
[Name]

8,8-difluoro-1,4-dioxaspiro[4.5]decane
[CAS]

176251-49-3
[Synonyms]

8,8-difluoro-1,4-dioxaspiro[4.5]decane
1,4-Dioxaspiro[4.5]decane, 8,8-difluoro-
[Molecular Formula]

C8H12F2O2
[MDL Number]

MFCD11847478
[MOL File]

176251-49-3.mol
[Molecular Weight]

178.18
Chemical PropertiesBack Directory
[Melting point ]

40-44 °C
[Boiling point ]

210.8±40.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

Store at room temperature
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C8H12F2O2/c9-7(10)1-3-8(4-2-7)11-5-6-12-8/h1-6H2
[InChIKey]

FLSBLABUGHZWBS-UHFFFAOYSA-N
[SMILES]

O1C2(CCC(F)(F)CC2)OCC1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2932990090
Spectrum DetailBack Directory
[Spectrum Detail]

8,8-difluoro-1,4-dioxaspiro[4.5]decane(176251-49-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,4-Dioxaspiro[4.5]decan-8-one

4746-97-8

8,8-difluoro-1,4-dioxaspiro[4.5]decane

176251-49-3

The general procedure for the synthesis of 8,8-difluoro-1,4-dioxaspiro[4.5]decane from 1,4-cyclohexanedione monoethyleneglycol ketal was as follows: method B: Ketone 6 (4.40 g, 28.2 mmol) was dissolved in anhydrous CH2Cl2 (100 mL) under argon gas protection and cooled to 0 °C. Morph-DAST (11.85 g, 67.7 mmol, 2.4 eq.) was slowly added dropwise under stirring conditions. Subsequently, the reaction mixture was gradually warmed to room temperature and stirred continuously for 72 hours. Upon completion of the reaction, saturated aqueous NaHCO3 (50 mL) was added to quench the unreacted fluoride and stirring was continued for 10 minutes. The organic layer was separated and the aqueous phase was extracted with CH2Cl2 (2 x 50 mL). An aqueous solution (100 mL) of KMnO4 (5.7 g, 36 mmol, 10 eq.) was added to the combined organic phases, and the suspension formed was reacted for 24 hours under vigorous stirring. The organic layer was separated again and the aqueous phase was extracted with CH2Cl2 (2 x 100 mL). All organic phases were combined and dried with Na2SO4, followed by vacuum evaporation of the solvent at 30 °C to give pure compound 7 (3.65 g, 20.5 mmol, 73% yield) as a colorless oil, which was stored and crystallized.

[References]

[1] Journal of Organic Chemistry, 2010, vol. 75, # 10, p. 3401 - 3411
[2] Organic Letters, 2013, vol. 15, # 5, p. 1088 - 1091
[3] Tetrahedron, 2013, vol. 69, # 20, p. 4066 - 4075
[4] Patent: US2003/149036, 2003, A1
[5] Journal of Fluorine Chemistry, 2013, vol. 153, p. 57 - 60
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