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61675-94-3

61675-94-3 Structure

61675-94-3 Structure
IdentificationBack Directory
[Name]

Ethyl 2-((Tetrahydro-2H-pyran-2-yl)oxy)acetate
[CAS]

61675-94-3
[Synonyms]

ethyl (tetrahydro-2H-pyran-2-yloxy)acetate
Ethyl 2-((Tetrahydro-2H-pyran-2-yl)oxy)acetate
[(Tetrahydropyran-2-yl)oxy]acetic acid ethyl ester
2-[(Tetrahydropyran-2-yl)oxy]acetic acid ethyl ester
O-(Tetrahydro-2H-pyran-2-yl)glycolic acid ethyl ester
Acetic acid, 2-[(tetrahydro-2H-pyran-2-yl)oxy]-, ethyl ester
[(Tetrahydropyran-2-yl)oxy]acetic acid ethyl ester O-(Tetrahydro-2H-pyran-2-yl)glycolic acid ethyl ester
[Molecular Formula]

C9H16O4
[MOL File]

61675-94-3.mol
[Molecular Weight]

188.22
Chemical PropertiesBack Directory
[Boiling point ]

88℃ (1 Torr)
[density ]

1.07±0.1 g/cm3(Predicted)
[refractive index ]

1.4440 (589.3 nm 16℃)
[storage temp. ]

2-8°C
[Appearance]

Colorless to light yellow Liquid
Hazard InformationBack Directory
[Uses]

Ethyl 2-((Tetrahydro-2H-pyran-2-yl)oxy)acetate has been used as a reactant for the sysnthesis of 3-phenylpyrazolo[1,5-a]pyrimidine as a potent corticotropin-releasing factor-1 antagonist.
[Synthesis]

3,4-Dihydro-2H-pyran

110-87-2

Ethyl glycolate

623-50-7

Ethyl 2-((Tetrahydro-2H-pyran-2-yl)oxy)acetate

61675-94-3

The general procedure for the synthesis of ethyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetate from 3,4-dihydro-2H-pyran and ethyl ethanoate was as follows: to a solution of toluene (100 mL) containing ethyl ethanoate (10 g, 0.0961 mol), 3,4-dihydro-2H-pyran (8 g, 0.096 mol) was added followed by catalytic amounts of p Toluenesulfonic acid (pTSA, 30 mg). The reaction mixture was stirred at 25°C for 1 hour. After completion of the reaction, the reaction mixture was washed sequentially with water and brine solution. The organic layer was separated, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford 18 g (99% yield) of ethyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetate as a colorless liquid.

[References]

[1] Patent: WO2017/83431, 2017, A2. Location in patent: Paragraph 00216; 00217
[2] Patent: US2011/87021, 2011, A1. Location in patent: Page/Page column 11
[3] Patent: US2005/8570, 2005, A1. Location in patent: Page/Page column 45
[4] Patent: WO2007/121453, 2007, A2. Location in patent: Page/Page column 111; 112
[5] Patent: US2010/239576, 2010, A1
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 2-((Tetrahydro-2H-pyran-2-yl)oxy)acetate(61675-94-3)1HNMR
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