ChemicalBook--->CAS DataBase List--->76757-90-9

76757-90-9

76757-90-9 Structure

76757-90-9 Structure
IdentificationBack Directory
[Name]

BOC-D-TYR-OME
[CAS]

76757-90-9
[Synonyms]

BOC-D-TYR-OME
BOC-D-TYROSINE-OME
Boc-D-Tyr-Ome, ≥97%
BOC-D-TYR-OME USP/EP/BP
BOC-D-TYROSINE METHYL ESTER
N-BOC-D-tyrosine methyl ester
N-T-boc-D-tyrosine methyl ester
(Tert-Butoxy)Carbonyl D-Tyr-OMe
Boc-D-tyrosine methyl ester≥ 98% (HPLC)
N-T-BUTOXYCARBONYL-D-TYROSINE METHYL ESTER
D-N-tert-Butoxycarbonyltyrosine methyl ester
D-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-,methyl ester
(R)-Methyl 2-((tert-butoxycarbonyl)aMino)-3-(4-hydroxyphenyl)propanoate
Methyl (R)-2-[(tert-Butoxycarbonyl)amino]-3-(4-hydroxyphenyl)propionate
methyl (2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-hydroxyphenyl)propanoate
methyl (2R)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
[EINECS(EC#)]

201-525-2
[Molecular Formula]

C15H21NO5
[MDL Number]

MFCD00057824
[MOL File]

76757-90-9.mol
[Molecular Weight]

295.33
Chemical PropertiesBack Directory
[Boiling point ]

452.7±40.0 °C(Predicted)
[density ]

1.169±0.06 g/cm3(Predicted)
[storage temp. ]

-15°C
[form ]

Powder
[pka]

9.75±0.15(Predicted)
[color ]

White
[InChI]

InChI=1S/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(18)20-4)9-10-5-7-11(17)8-6-10/h5-8,12,17H,9H2,1-4H3,(H,16,19)/t12-/m1/s1
[InChIKey]

NQIFXJSLCUJHBB-GFCCVEGCSA-N
[SMILES]

C(OC)(=O)[C@@H](CC1=CC=C(O)C=C1)NC(OC(C)(C)C)=O
[CAS DataBase Reference]

76757-90-9
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P261-P280-P305+P351+P338-P304+P340-P405-P501
[WGK Germany ]

3
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

peptide synthesis
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

H-D-TYR-OME HCL

3728-20-9

BOC-D-TYR-OME

76757-90-9

General procedure for the synthesis of butoxycarbonyl-D-tyrosine-methoxylate from di-tert-butyl dicarbonate and (R)-2-amino-3-(4-hydroxyphenyl)propanoic acid methyl ester hydrochloride: potassium carbonate (250.9 g, 1.815 mol) was added to 1.0 L of water with stirring, and under ice-water-bath conditions, (R)-2-amino-3-(4-hydroxyphenyl)propanoic acid methyl ester hydrochloride ( 140.2 g, 0.605 mol), and then di-tert-butyl dicarbonate (158.4 g, 0.726 mol) was added slowly and dropwise. Ethanol (300 mL) was then added. After the dropwise addition, the reaction mixture was naturally warmed to room temperature and stirred for 2 h. The progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, extraction was carried out with ethyl acetate (600 mL × 3), the organic phases were combined and washed sequentially with 1N hydrochloric acid (400 mL), water (400 mL) and saturated brine (400 mL × 2), and the organic phase was dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to obtain a solid product, washed with 300 mL of hexane, and dried to give 175.8 g of white solid product in 98.4% yield.

[References]

[1] Organic Letters, 2002, vol. 4, # 2, p. 265 - 267
[2] Patent: CN105777584, 2016, A. Location in patent: Paragraph 0114; 0115; 0116
[3] Journal of Organic Chemistry, 2000, vol. 65, # 16, p. 5037 - 5042
[4] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1997, vol. 36, # 7, p. 562 - 565
[5] Journal of Organic Chemistry, 1981, vol. 46, # 9, p. 1944 - 1946
Spectrum DetailBack Directory
[Spectrum Detail]

BOC-D-TYR-OME(76757-90-9)1HNMR
BOC-D-TYR-OME(76757-90-9)1HNMR
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