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

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Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:4-Methyltetrahydropyran-4-carboxylic Acid
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CAS:233276-38-5
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2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI) manufacturers

2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI) Basic information
Product Name:2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI)
Synonyms:2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI);4-Methyltetrahydro-2H-pyran-4-carboxylic acid;4-Methyltetrahydro-2H-pyr...;4-Methyltetrahydropyran-4-carboxylic Acid;4-Methyloxane-4-carboxylic acid;2H-Pyran-4-carboxylicacid,tetrahydro-4-Methyl-;Tetrahydro-4-methyl-2H-pyran-4-carboxylic acid
CAS:233276-38-5
MF:C7H12O3
MW:144.17
EINECS:
Product Categories:CARBOXYLICACID
Mol File:233276-38-5.mol
2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI) Structure
2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI) Chemical Properties
Boiling point 257℃
density 1.124
Fp 105℃
storage temp. Sealed in dry,Room Temperature
pka4.56±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2932990090
MSDS Information
2H-Pyran-4-carboxylicacid,tetrahydro-4-methyl-(9CI) Usage And Synthesis
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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