ChemicalBook--->CAS DataBase List--->929019-95-4

929019-95-4

929019-95-4 Structure

929019-95-4 Structure
IdentificationBack Directory
[Name]

6-(HYDROXYMETHYL)MORPHOLIN-3-ONE
[CAS]

929019-95-4
[Synonyms]

6-(HYDROXYMETHYL)MORPHOLIN-3-ONE
3-Morpholinone, 6-(hydroxymethyl)-
[Molecular Formula]

C5H9NO3
[MOL File]

929019-95-4.mol
[Molecular Weight]

131.13
Chemical PropertiesBack Directory
[Boiling point ]

397.1±27.0 °C(Predicted)
[density ]

1?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.98±0.40(Predicted)
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

6-(HYDROXYMETHYL)MORPHOLIN-3-ONE(929019-95-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Chloro-N-(2,3-dihydroxypropyl)acetaMide

71064-34-1

6-(HYDROXYMETHYL)MORPHOLIN-3-ONE

929019-95-4

Step-2: Potassium tert-butoxide (23.4 g, 299.4 mmol) was dissolved in 200 mL of tert-amyl alcohol under nitrogen protection and stirred at room temperature. Subsequently, a solution of 2-chloro-N-(2,3-dihydroxypropyl)acetamide (Step-1 product of Intermediate-9) (20 g, 119.6 mmol) dissolved in 460 mL of tert-amyl alcohol was added to this solution and the reaction lasted for 2 hours. After 1 hour of reaction, methanol (100 mL) and water (3 mL) were added and stirring was continued for 20 minutes. Upon completion of the reaction, the reaction mixture was concentrated under vacuum and purified by rapid chromatography on silica gel using methanol/ethyl acetate (20:80) as eluent to afford 6-(hydroxymethyl)morpholin-3-one as a white solid (14.4 g). Mass spectral data: m/z 132.1.

[References]

[1] Patent: US2011/82138, 2011, A1. Location in patent: Page/Page column 80
[2] Patent: WO2012/120476, 2012, A1. Location in patent: Page/Page column 62
[3] Patent: US2013/345213, 2013, A1. Location in patent: Paragraph 0366
[4] Journal of Medicinal Chemistry, 2018, vol. 61, # 11, p. 4832 - 4850
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