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[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester

[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Suppliers list
Company Name: Chengdu HappySyn Pharmaceutical Technology Co., Ltd.  
Tel: 85114309 18982182443
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[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester manufacturers

[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Basic information
Product Name:[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester
Synonyms:Carbamic acid, N-[4-(2-aminoethyl)phenyl]-, 1,1-dimethylethyl ester;4-(2-Aminoethyl)-N-Boc-aniline;tert-Butyl (4-(2-aminoethyl)phenyl)carbamate;[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester
CAS:457631-44-6
MF:C13H20N2O2
MW:236.31
EINECS:
Product Categories:
Mol File:457631-44-6.mol
[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Structure
[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Chemical Properties
Melting point 89-91 °C
Boiling point 315.9±25.0 °C(Predicted)
density 1.099±0.06 g/cm3(Predicted)
storage temp. Store at Room Tem.
pka13.79±0.70(Predicted)
Appearancewhite to off-white solid
Safety Information
MSDS Information
[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Usage And Synthesis
Synthesis[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester is synthesised using 4-tert-butoxycarbonylaminophenylacetonitrile as a raw material by chemical reaction. The specific synthesis steps are as follows:
To a solution of (300 gm, 1.29 moles) N-BOC-4-aminophenylacetonitrile in 3000 ml of methanol, 25% aq. ammonia solution (480 ml) and Raney nickel (45 gm) were added at 25 -30°C. Reaction mixture was subjected to hydrogenation at 50-60 PSI for 4 hrs. After completion of reaction, as indicated from TLC, reaction mixture was filtered and washed with (2 X 25 ml) methanol. Filtrate was concentrated under vacuum and resulting residue was treated with (1500 ml) 1M aq. hydrochloric acid at 25-30°C. Reaction mixture was stirred for 15 minutes and filtered to remove insoluble impurities. Filtrate was basified to pH 10-12 with 50% aq. NaOH solution below 25°C. Precipitated 4-(2-aminoethyl)-N-(tert-butoxycarbonyl) phenylamine was filtered and washed with (2 X 100 ml) water. Solid was dried under vacuum at 55- 60°C for 8-10 hrs. Dry weight: 240 gm (79%). 1H NMR (CDC13 and 400 MHz): δ 1.11 (2H, s), 1.51 (9H, s), 2.68 (2H, t), 2.93 (2H, t), 6.72 (1H, s), 7.10 (2H, d), 7.28 (2H, d).
[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester synthesis
[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Preparation Products And Raw materials
Tag:[4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester(457631-44-6) Related Product Information
tert-Butyl 4-(2-oxo-2-piperazin-1-ylethyl)phenylcarbamate [4-(2-Amino-ethyl)-phenyl]-carbamic acid tert-butyl ester Boc-L-Phe(4-nh-Boc) Fmoc-Phe(4-NHBoc,3,5-i 2)-OH H-Phe(4-nh-Boc)-OH (S)-N-9-Fluorenylmethyloxycarbonyl-7-(N'-t-butyloxycarbonyl-amino)-[1,2,3,4]-tetrahydroisoquinoline-3-carboxylix acid Boc-D-Phe(4-NHBoc)-OH (4-Piperidin-3-yl-phenyl)-carbamic acid tert-butyl ester 2-tert-Butoxycarbonylamino-3-(4-tert-butoxycarbonylamino-phenyl)-propionic acid (S)-N-alpha-t-Butyloxycarbonyl-4-(t-butyloxycarbonyl-amido)-phenylalanine benzyl ester Fmoc-p(NH-Boc)-L-Phe-OH Tert-butyl 1,2,3,4-tetrahydroisoquinolin-7-ylcarbamate tert-butyl 4-(pyrrolidin-3-yl)phenylcarbamate Tert-butyl indolin-6-yl-carbamate