ChemicalBook--->CAS DataBase List--->156939-62-7

156939-62-7

156939-62-7 Structure

156939-62-7 Structure
IdentificationBack Directory
[Name]

(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate
[CAS]

156939-62-7
[Synonyms]

Fmoc-Gly-al
N-9-Fluorenylmethoxycarbonylglycinaldehyde
(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate
9H-fluoren-9-ylmethyl N-(2-oxoethyl)carbamate
2-[[(9-Fluorenylmethoxy)carbonyl]amino]acetaldehyde
Carbamic acid, N-(2-oxoethyl)-, 9H-fluoren-9-ylmethyl ester
[Molecular Formula]

C17H15NO3
[MDL Number]

MFCD11519176
[MOL File]

156939-62-7.mol
[Molecular Weight]

281.31
Chemical PropertiesBack Directory
[Melting point ]

141.0-143.0℃
[Boiling point ]

477.5±28.0 °C(Predicted)
[density ]

1.230±0.06 g/cm3(Predicted)
[storage temp. ]

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

10.72±0.46(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

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

(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate(156939-62-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Fmoc-Glycinol

105496-31-9

(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate

156939-62-7

General procedure for the synthesis of N-fluorenylmethoxycarbonylglyceraldehyde from 2-(N-fluorenylmethoxycarbonylamino)ethanol: Diisopropylethylamine (12.4 mL, 70.6 mmol) was added to a dichloromethane (50 mL) suspension of 2-(N-fluorenylmethoxycarbonylamino)ethanol (5.0 g, 18 mmol). The reaction mixture was cooled to -40 °C and a solution of sulfur trioxide pyridine complex (11.2 g, 70.6 mmol) in dimethyl sulfoxide (49.5 mL) was added dropwise over 15 min. After continuous stirring at -40 °C for 1 h, the reaction was quenched with a mixture of ice water and saturated saline. The organic solvent was removed by concentration under reduced pressure, and the resulting off-white precipitate was collected by filtration and dried under vacuum. Finally, purification was carried out by silica gel fast column chromatography to afford N-fluorenylmethoxycarbonylglyceraldehyde (4.7 g, 94% yield) using ethyl acetate/hexane (1:1, v/v) as eluent.

[References]

[1] Organic Letters, 2002, vol. 4, # 17, p. 3001 - 3003
[2] Synthetic Communications, 2007, vol. 37, # 20, p. 3493 - 3499
[3] Patent: WO2018/149419, 2018, A1. Location in patent: Paragraph 001283; 001284
[4] European Journal of Organic Chemistry, 2008, # 34, p. 5786 - 5797
[5] Patent: WO2006/66183, 2006, A2. Location in patent: Page/Page column 63
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