Home Cart Sign in  
Chemical Structure| 67630-00-6 Chemical Structure| 67630-00-6

Structure of Boc-Phe(4-NO2)-OEt
CAS No.: 67630-00-6

Chemical Structure| 67630-00-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 67630-00-6 ]

CAS No. :67630-00-6
Formula : C16H22N2O6
M.W : 338.36
SMILES Code : O=C(OCC)[C@@H](NC(OC(C)(C)C)=O)CC1=CC=C([N+]([O-])=O)C=C1
MDL No. :MFCD18207035
InChI Key :KVEDDVRFINSSND-ZDUSSCGKSA-N
Pubchem ID :10593086

Safety of [ 67630-00-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 67630-00-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 67630-00-6 ]

[ 67630-00-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67630-00-6 ]
  • [ 67630-01-7 ]
YieldReaction ConditionsOperation in experiment
89% With hydrogen;palladium 10% on activated carbon; In ethanol; under 2068.65 - 2585.81 Torr; for 1h; A solution of N-BOC-4-nitro-L-phenyl alanine ethyl ester (78.3 g, 0.22 mol) in absolute ethanol (300 mL) was purged with nitrogen, and 10% palladium on carbon (1.0 g) was added. After hydrogenated at 40-50 psi for 1 h, the reaction mixture was filtered through Celite, and the cake was washed with EtOH followed by EtOAc. The filtrate was concentrated, and the residue was purified by flash column chromatography on silica gel eluting with 4:1 to 1:1 EtOAc/Hexanes to afford the title compound (60 g 89% yield). lH NMR (400 MHz, CDCI3) delta 6.90 (d, 2H), 6.63 (d, 2H), 4.20-4.50 (m,lH), 4.14 (q, 2H), 3.76-3.00 (m, 2H), 1.36 (s, 9H).1.20 (t, 3H).
With hydrogen;palladium 10% on activated carbon; In ethanol; under 2068.65 - 2585.81 Torr; for 1h; Step C : A solution of the compound of Step B (78. 3 g, 0. 22 mol) in absolute ethanol (300 mL) was purged with nitrogen, and 10% palladium on carbon (1. 0 g) was added. After hydrogenated at 40-50 psi for 1 h, the reaction mixture was filtered through Celite, and the cake was washed with EtOH followed by EtOAc. The filtrate was concentrated, and the residue was purified by flash column chromatography on silica gel eluting with 4 : 1 to 1 : 1 EtOAc/Hexanes to afford N-BOC-4-amino-L-phenylalanine, ethyl ester (60 g). 1H NMR (400 MHz, Cd13) 8 6. 90 (d, 2H), 6. 63 (d, 2H), 4. 20-4. 50 (m, lH), 4. 14 (q, 2H), 3. 76-3. 00 (m, 2H), 1. 36 (s, 9H), 1. 20 (t, 3H).
palladium-carbon; In ethanol; (9-1) In 120 ml of ethanol was dissolved 4.95 g (14.6 mmol) of N-t-butoxycarbonyl-DL-4-nitrophenylalanine ethyl ester, and 500 mg of 10% palladium carbon was added to the solution and the mixture was stirred under hydrogen atmosphere at 50-60 C. for 6 hours. The resulting reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by the silica gel column chromatography ethod (eluent: chloroform/ethyl acetate=50/1) to obtain 3.97 g (12.8 mmol) of N-t-butoxycarbonyl-DL-4-aminophenylalanine ethyl ester as white solid. 1H-NMR (CDCl3) delta; 6.92 (d, J=8 Hz, 2H), 6.63 (d, J=8 Hz, 2H), 5.03-4.85 (m, 1H), 4.56-4.38 (m, 1H), 4.16 (q, J=7.3 Hz, 2H), 3.15-2.82 (m, 2H), 1.42 (s, 9H), 1.25 (t, J=7.3 Hz, 3H). CI-MS (m/z); 253
With hydrogen;10% palladium on activated carbon; In ethanol; The mixture of 4.6 g of Boc-Phe(4-NO2)-Oet, 900 mg of 10% palladium charcoal (containing 50% water) and ethanol was stirred overnight under the hydrogen atmosphere. After Celite filtration, the solvent was removed to obtain the objective compound. Yield: 4.4 g H-NMR (CDCl3) delta 1. 25 (3H, t), 1. 40 (9H, s), 2. 95 (2H, br), 4. 15 (2H, q), 4.45 (1H, m), 4.95 (1H, br), 6.60 (2H, d), 6.95 (2H, d).
With hydrogen;palladium on carbon; In N,N-dimethyl-formamide; for 8h;Product distribution / selectivity; 3) Hydrogen conversion reaction of Boc-3-(4-nitro-phenyl)-2-tert-butoxycarbonylamino-propionic acid ethyl ester (Boc-ntrPhe-OEt) 1 g of Boc-ntrPhe-OEt, 30 ml of DMF and 0.05 g of palladium-carbon (Pd-C) were mixed, gas-filling by hydrogen was conducted using a balloon, and the solution was stirred for approximately 8 hours. During the stirring, hydrogen was changed every 2 hours. The product was analyzed by 1H-NMR spectroscopy.
With palladium 10% on activated carbon; hydrogen; In methanol; The intermediate (17) was dissolved in methanol, 10% Pd / C was added, and the hydrogen was pressurized. Filtered, concentrated under reduced pressure to the give intermediate (18).
With palladium 10% on activated carbon; hydrogen; In N,N-dimethyl-formamide; at 50℃;Inert atmosphere; Large scale; N-tert-butoxycarbonyl-L-4-nitrophenylalanine ethyl ester (3.385 kg, 10.0 mol) was added to a 100 L enamel kettle containing N,N-dimethylformamide (26 L).Stir and dissolve until clear, add 10% Pd on carbon (170g), replace with nitrogen three times, replace with hydrogen three times, heat up to 50C and continue to pass hydrogen,After sampling and detecting the reaction of N-tert-butoxycarbonyl-L-4-nitrophenylalanine ethyl ester, the hydrogen gas was stopped and the reaction was allowed to come to room temperature, filtered, and the mother liquor was directly used in the next step.

 

Historical Records

Technical Information

Categories