ChemicalBook--->CAS DataBase List--->82911-79-3

82911-79-3

82911-79-3 Structure

82911-79-3 Structure
IdentificationBack Directory
[Name]

FMOC-TYR-OME
[CAS]

82911-79-3
[Synonyms]

FMOC-TYR-OME
Fmoc-L-Tyr-OMe
N-Fmoc-L-tyrosine methyl ester
METHYL D-AMINOLEVULINATE HYDROCHLORIDE
(9H-Fluoren-9-yl)MethOxy]Carbonyl Tyr-OMe
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tyrosine methyl ester
L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, methyl ester
(S)-Methyl 2-((((9H-fluoren-9-yl)Methoxy)carbonyl)aMino)-3-(4-hydroxyphenyl)propanoate
methyl (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(4-hydroxyphenyl)propanoate
[Molecular Formula]

C25H23NO5
[MOL File]

82911-79-3.mol
[Molecular Weight]

417.45
Chemical PropertiesBack Directory
[Melting point ]

122-123 °C
[Boiling point ]

645.2±55.0 °C(Predicted)
[density ]

1.275±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

9.75±0.15(Predicted)
[Appearance]

White to off-white Solid
[Optical Rotation]

32.668° (C=0.01 g/ml, CHCL3)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

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

FMOC-TYR-OME(82911-79-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(triphenylmethyl)-, methyl ester

1240497-07-7

FMOC-TYR-OME

82911-79-3

GENERAL PROCEDURE: METHOD A-USE OF PLANETARY BALL MILL: Triphenylmethylated compounds (1 mmol; typically 563 mg, 4) and In(OTf)3 (141 mg, 0.25 mmol) were mixed in a 50 mL stainless steel (SS) jar with ten 10-mm diameter SS balls. The reaction was carried out in a planetary ball mill (PM-100) at 550 rpm for 3.5 h (the progress of the reaction was monitored by TLC and the unfolding agent was EtOAc:Hex, 1:1). Upon completion of the reaction, EtOAc was added to the mixture and the solution was transferred to a dispensing funnel (50 ml × 3). The organic phase was washed sequentially with 10% Na2CO3 aqueous solution (50 ml × 2) and water (50 ml), dried with Na2SO4 and concentrated under reduced pressure to obtain the crude de-O-tritylated product. The crude product was purified by fast chromatography to remove the by-product TrOH to give the pure product (yield: 305 mg, 95.2%, 5 from 4). The pure product was crystallized from ether-n-Hex to give an analytically pure product. The spectral data of the product was in agreement with the expected structure and literature values. Method B-Use of a Vibratory Ball Mill: the triphenylmethylated compound (1 mmol; typically 563 mg, 4) and In(OTf)3 (141 mg, 0.25 mmol) were mixed in a 10 mL stainless steel (SS) jar to which 20 SS balls of 3 mm diameter were added. The reaction was carried out in a vibrating ball mill (MM-400) at 30 Hz for 15 min (the progress of the reaction was monitored by TLC and the unfolding agent was EtOAc/Hex, 1:1). The post-treatment and isolation steps of the product were the same as in Method A. The yield was 308 mg, 96.2%, from 4 to 5.

[References]

[1] Carbohydrate Research, 2014, vol. 397, p. 18 - 26
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