ChemicalBook--->CAS DataBase List--->23462-75-1

23462-75-1

23462-75-1 Structure

23462-75-1 Structure
IdentificationBack Directory
[Name]

2H-PYRAN-3(4H)-ONE, DIHYDRO-
[CAS]

23462-75-1
[Synonyms]

oxan-3-one
2H-PYRAN-3(4H)-ONE
DIHYDRO-PYRAN-3-ONE
Tetrahydropyran-3-One
tetrahydro-2H-3-pyranone
Tetrahydro-2H-pyran-3-one
2H-PYRAN-3(4H)-ONE, DIHYD...
2H-PYRAN-3(4H)-ONE, DIHYDRO-
2H-Pypan-3(4H)-one, dihydro-
5,6-Dihydro-2H-pyran-3(4H)-one
Dihydro-2H-pyran-3(4H)-one, 95+%
2H-PYRAN-3(4H)-ONE, DIHYDRO- ISO 9001:2015 REACH
[EINECS(EC#)]

813-813-8
[Molecular Formula]

C5H8O2
[MDL Number]

MFCD00182426
[MOL File]

23462-75-1.mol
[Molecular Weight]

100.12
Chemical PropertiesBack Directory
[Boiling point ]

55 °C(Press: 12 Torr)
[density ]

1.0856 g/cm3
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

liquid
[color ]

Colourless
[InChI]

InChI=1S/C5H8O2/c6-5-2-1-3-7-4-5/h1-4H2
[InChIKey]

URUUZIAJVSGYRC-UHFFFAOYSA-N
[SMILES]

C1OCCCC1=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P312
[HazardClass ]

IRRITANT
[HS Code ]

2932990090
Hazard InformationBack Directory
[Uses]

Dihydro-?2H-?pyran-?3(4H)?-?one is a general chemical reagent used in the synthesis of pharmaceuticals such as the preparation of tetrahydropyran-2-yl chromans, a highly selective beta-site amyloid precursor protein cleaving enzyme 1 (BACE) inhibitor.
[Synthesis]

TETRAHYDRO-2H-PYRAN-3-OL

19752-84-2

2H-PYRAN-3(4H)-ONE, DIHYDRO-

23462-75-1

The general procedure for the synthesis of dihydro-2H-pyran-3(4H)-ones using 3-hydroxytetrahydropyran as starting material was as follows: 3-hydroxytetrahydropyran (300 g, 2.9 mol) was dissolved in dichloromethane (3,000 g), followed by the addition of sodium acetate (287 g, 3.5 mol) and TEMPO (6 g). Sodium dichloroisocyanurate (374 g, 1.7 mol) was added in batches at 25 °C and the reaction temperature was maintained at 25 °C for a continuous period of 2 hours. After completion of the reaction, filtration was carried out and the organic phase was dried with anhydrous sodium sulfate (200 g). After filtration again, it was concentrated under reduced pressure using a rotary evaporator and distilled to collect a fraction with an oil bath temperature of 120 °C and a top temperature of 90 °C of the distillate. The final product was obtained as a colorless oily liquid which was tested to be 99% pure and 83% yield.

[References]

[1] Heterocycles, 2011, vol. 82, # 2, p. 1267 - 1282
[2] Patent: CN107382928, 2017, A. Location in patent: Paragraph 0007-0008; 0010-0011; 0013-0014
[3] Liebigs Annalen der Chemie, 1983, # 11, p. 1950 - 1958
[4] Tetrahedron, 2003, vol. 59, # 9, p. 1453 - 1467
[5] Patent: CN104650049, 2018, B. Location in patent: Paragraph 0603; 0604
Spectrum DetailBack Directory
[Spectrum Detail]

2H-PYRAN-3(4H)-ONE, DIHYDRO-(23462-75-1)1HNMR
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