Home Cart Sign in  
Chemical Structure| 14719-37-0 Chemical Structure| 14719-37-0
Chemical Structure| 14719-37-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Boc-Gly-OEt is a glycine derivative with Boc protection of the amino group and ethyl esterification of the carboxyl group, widely used in peptide synthesis to prevent unwanted reactions.

Synonyms: Ethyl (tert-Butoxycarbonyl)glycinate

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 Boc-Gly-OEt

CAS No. :14719-37-0
Formula : C9H17NO4
M.W : 203.24
SMILES Code : O=C(OCC)CNC(OC(C)(C)C)=O
Synonyms :
Ethyl (tert-Butoxycarbonyl)glycinate
MDL No. :MFCD05663720
InChI Key :CNIBHMMDDXGDNR-UHFFFAOYSA-N
Pubchem ID :357729

Safety of Boc-Gly-OEt

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of Boc-Gly-OEt

* 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 [ 14719-37-0 ]

[ 14719-37-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 14719-37-0 ]
  • [ 140-88-5 ]
  • [ 146256-98-6 ]
YieldReaction ConditionsOperation in experiment
To a suspensionof sodium hydride (60 percent, 18.4 g, 768.47 mmol) in toluene (350 mL) at 0 °C was added portion wise Intermediate 11 (120 g, 591.13 mmol). After stirring for 5 h at this temperature, to the mixture was added drop wise ethyl acrylate (76.8 g, 768.47 mmol). After additional stirring for 2 h at rt, the reaction was quenched with water (200 mL) carefully and extracted with EtOAc (600 mL X 2). The combined extract was dried over anhydrous sodium sulfate, concentrated to afford crude Intermediate 12 (50 g, 33percent yield, pale brown liquid).JH NMR (400 MHz, CDCb)
  • 2
  • [ 14719-37-0 ]
  • [ 676-58-4 ]
  • [ 183059-24-7 ]
YieldReaction ConditionsOperation in experiment
With ammonium chloride; In tetrahydrofuran; STR65 Ethyl 2-(tert-butoxycarbonylamino)acetate (4.17 g, 20.52 mmol) was dissolved in tetrahydrofuran (60 ml). The solution was cooled to -78 C. A 22% solution of methyl magensium chloride in toluene/tetrahydrofuran (purchased from Chemmetallgesellschaft, 27.1 ml, 67.72 mmol) was added dropwise. The reaction mixture was stirred for 1.5 h at -78 C. and then warmed to room temperature. A 10% aqueous solution of ammonium chloride (200 ml) was added dropwise. The phases were separated. The aqueous phase was extracted with ethyl acetate (3*100 ml). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (200 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (110 g), using ethyl acetate/heptane (1:1) as eluent, to give 1.31 g of 2-hydroxy-2-methylpropylcarbamic acid tert-butyl ester. 1 H-NMR (CDCl3): d 1.21 (s, 6 H); 1.45 (s, 9 H); 1.34 (d, 2 H); 5.00 (br, 1H).
 

Historical Records

Technical Information

Categories