ChemicalBook--->CAS DataBase List--->233276-38-5

233276-38-5

233276-38-5 Structure

233276-38-5 Structure
IdentificationBack Directory
[Name]

2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI)
[CAS]

233276-38-5
[Synonyms]

4-Methyltetrahydro-2H-pyr...
4-Methyloxane-4-carboxylic acid
4-Methyltetrahydropyran-4-carboxylic Acid
4-Methyltetrahydro-2H-pyran-4-carboxylic acid
2H-Pyran-4-carboxylicacid,tetrahydro-4-Methyl-
Tetrahydro-4-methyl-2H-pyran-4-carboxylic acid
2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI)
[Molecular Formula]

C7H12O3
[MDL Number]

MFCD11977785
[MOL File]

233276-38-5.mol
[Molecular Weight]

144.17
Chemical PropertiesBack Directory
[Boiling point ]

257℃
[density ]

1.124
[Fp ]

105℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.56±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HS Code ]

2932990090
Spectrum DetailBack Directory
[Spectrum Detail]

2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI)(233276-38-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-,methylester(9CI)

443912-70-7

2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI)

233276-38-5

The general procedure for the synthesis of 4-methyltetrahydropyran-4-carboxylic acid from methyl 4-methyl-tetrahydro-2H-pyran-4-carboxylate was as follows: to a solution of methyl 4-methyltetrahydro-2H-pyran-4-carboxylate (5.00 g, 31.6 mmol) in a 1:1:1 mixed solvent of dioxane/water/methanol (60 mL), lithium hydroxide hydrate (5.31 g, 126 mmol) and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was partially concentrated and subsequently diluted with water and ethyl acetate (EtOAc) and acidified with 6 M hydrochloric acid to pH=1. The organic and aqueous layers were separated and the aqueous layer was extracted with additional ethyl acetate (50 mL). All organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to dryness to afford 4-methyltetrahydro-2H-pyran-4-carboxylic acid (4.61 g, 100% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 12.29 (s, 1H), 3.65 (dt, J=11.8,4.3 Hz, 2H), 3.33-3.32 (m, 2H), 1.87-1.86 (m, 2H), 1.35 (ddd, J=13.5,9.9,4.1 Hz, 2H). 1.13 (s, 3H).

[References]

[1] Patent: US2014/275016, 2014, A1. Location in patent: Paragraph 0266
[2] Patent: US2014/275080, 2014, A1. Location in patent: Paragraph 0400
[3] ChemMedChem, 2010, vol. 5, # 1, p. 65 - 78
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