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18144-47-3

18144-47-3 Structure

18144-47-3 Structure
IdentificationMore
[Name]

tert-Butyl 4-aminobenzoate
[CAS]

18144-47-3
[Synonyms]

4-AMINOBENZOIC ACID TERT-BUTYL ESTER
BUTTPARK 14\02-67
TERT-BUTYL 4-AMINOBENZOATE
[EINECS(EC#)]

629-537-4
[Molecular Formula]

C11H15NO2
[MDL Number]

MFCD00665790
[Molecular Weight]

193.24
[MOL File]

18144-47-3.mol
Chemical PropertiesBack Directory
[Melting point ]

108-110 °C
[Boiling point ]

322.4±15.0 °C(Predicted)
[density ]

1.078±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

2.43±0.10(Predicted)
[color ]

White to Light yellow to Light orange
[BRN ]

2803178
[Major Application]

peptide synthesis
[InChI]

InChI=1S/C11H15NO2/c1-11(2,3)14-10(13)8-4-6-9(12)7-5-8/h4-7H,12H2,1-3H3
[InChIKey]

KYORUZMJUKHKFS-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)C1=CC=C(N)C=C1
[CAS DataBase Reference]

18144-47-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[F ]

10-34
[Hazard Note ]

Irritant
[HS Code ]

29224999
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

tert-Butyl 4-aminobenzoate(18144-47-3) can be used to synthesise structural units for antifolate and a novel liver-targeted coupling of PSN-357, a glycogen phosphorylase inhibitor for the treatment of diabetes. It can also be used in the synthesis of tert-butyl 4-aminobenzoate n-substituted derivatives[1].
[reaction suitability]

reaction type: solution phase peptide synthesis
[Synthesis]

tert-Butyl 4-aminobenzoate(18144-47-3) is synthesised using tert-butyl 4-nitrobenzoate as raw material by chemical reaction. The specific synthesis steps are as follows:
Tert-butyl 4-nitrobenzoate (4.75 g, 21.279 mmol) was dissolved in MeOH (200 ml) and added with CAUTION was Pd/C (475 mg, 0.1 equiv. w/w) and the flask evacuated prior to purging with N2, re-evacuation and purging with H2. The mixture was stirred under H2 for 5 hours until complete. The mixture was filtered through celite and evaporated to a white solid (4.11 g, 21.269 mmol, quant.). Rf 0.29 [20% EtOAc in Hexane]. Mp. I l l - 113 0C. 1H NMR (400 MHz, CDCl3) δ 7.79 (2H, dt, J=8.6, 2.3 Hz, 2ArH), 6.61 (2H, dt, J=8.6, 2.3 Hz, 2ArH), 4.00 (2H, br s, NH2), 1.56 (9H, s, C(CH3)3) ppm. 13C NMR (100 MHz, CDCl3) δ 165.9 (C=O), 150.4 (ArC), 131.3 (ArCH), 121.7 (ArC), 113.7 (ArCH), 80.0 (C(CH3)3), 28.3 (C(CH3)3) ppm. IR (neat) υmax 3415, 3345, 3235, 2972, 1682, 1598, 1367, 1287, 1154, 1115 cm 1. HRMS mJz calc. C11H15NO2 [M+l] 194.1176, found [M+l] 194.1179.
tert-Butyl 4-aminobenzoate synthesis
[References]

[1] V. BAVETSIAS  E. H. Synthesis of N-substituted derivatives of tert-butyl 4-aminobenzoate via a palladium-catalysed reaction[J]. Journal of Chemical Research-s, 2000. DOI:10.3184/030823400103168100.
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 4-aminobenzoate(18144-47-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

18144-47-3(sigmaaldrich)
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