ChemicalBook--->CAS DataBase List--->122665-97-8

122665-97-8

122665-97-8 Structure

122665-97-8 Structure
IdentificationMore
[Name]

4,4-Difluorocyclohexanecarboxylic acid
[CAS]

122665-97-8
[Synonyms]

4,4-DIFLUOROCYCLOHEXANECARBOXYLIC ACID
Cyclohexanecarboxylic acid, 4,4-difluoro-
4,4-DIFLUOROCYCLOHEXYLCARBOXYLIC ACID
[EINECS(EC#)]

602-802-1
[Molecular Formula]

C7H10F2O2
[MDL Number]

MFCD03788493
[Molecular Weight]

164.15
[MOL File]

122665-97-8.mol
Chemical PropertiesBack Directory
[Melting point ]

103-107 °C
[Boiling point ]

241.1±40.0 °C(Predicted)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

Chloroform, Methanol
[form ]

Solid
[pka]

4.06±0.10(Predicted)
[color ]

White
[InChI]

InChI=1S/C7H10F2O2/c8-7(9)3-1-5(2-4-7)6(10)11/h5H,1-4H2,(H,10,11)
[InChIKey]

HYIUDFLDFSIXTR-UHFFFAOYSA-N
[SMILES]

C1(C(O)=O)CCC(F)(F)CC1
[CAS DataBase Reference]

122665-97-8(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29161900
Hazard InformationBack Directory
[Chemical Properties]

4,4-Difluorocyclohexanecarboxylic acid is White Solid
[Uses]

4,4-Difluorocyclohexanecarboxylic acid is a di-substituted cyclohexane carboxylic acids used in the synthesis of macrolide antibiotics.
[Synthesis]

ETHYL 4,4-DIFLUOROCYCLOHEXANECARBOXYLATE

178312-47-5

4,4-Difluorocyclohexanecarboxylic acid

122665-97-8

The general procedure for the synthesis of 4,4-difluorocyclohexanecarboxylic acid from ethyl 4,4-difluorocyclohexanecarboxylate was as follows: ethyl 4,4-difluorocyclohexanecarboxylate (0.385 g, 2.003 mmol) was dissolved in THF (12 mL), and H2O (6 mL) was added, followed by lithium hydroxide monohydrate (0.420 g, 10.02 mmol). The reaction mixture was stirred vigorously at room temperature overnight. Upon completion of the reaction, the mixture was diluted with EtOAc and the pH was adjusted to 4 with 1 M HCl. The organic and aqueous layers were separated, and the aqueous layer was then extracted with EtOAc (1 time). The organic phases were combined, washed with brine, dried over MgSO4 and concentrated to dryness to give 4,4-difluorocyclohexanecarboxylic acid (318 mg, 97% yield) as a white solid.1H NMR (400 MHz, DMSO-d6): δ 12.28 (s, 1H), 2.40 (m, 1H), 2.02-1.75 (m, 6H), 1.59 (m, 2H) .

[References]

[1] Patent: US2014/275080, 2014, A1. Location in patent: Paragraph 0428
[2] Patent: WO2013/13188, 2013, A1. Location in patent: Paragraph 00313; 00314
[3] Patent: US9416132, 2016, B2. Location in patent: Page/Page column 134; 135
[4] Organic Letters, 2018, vol. 20, # 16, p. 4959 - 4963
[5] Patent: US2008/146605, 2008, A1. Location in patent: Page/Page column 39-40
Spectrum DetailBack Directory
[Spectrum Detail]

4,4-Difluorocyclohexanecarboxylic acid(122665-97-8)1HNMR
4,4-Difluorocyclohexanecarboxylic acid(122665-97-8)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4,4-Difluorocyclohexanecarboxylic acid, 98%(122665-97-8)
[Sigma Aldrich]

122665-97-8(sigmaaldrich)
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