Home Cart Sign in  
Chemical Structure| 51077-13-5 Chemical Structure| 51077-13-5

Structure of 51077-13-5

Chemical Structure| 51077-13-5

*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 [ 51077-13-5 ]

CAS No. :51077-13-5
Formula : C10H15NO4
M.W : 213.23
SMILES Code : O=C(C1N(C(OC(C)(C)C)=O)CC=C1)O
MDL No. :MFCD10686611

Safety of [ 51077-13-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 51077-13-5 ]

* 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 [ 51077-13-5 ]

[ 51077-13-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 23357-46-2 ]
  • [ 51077-13-5 ]
  • [ 876624-17-8 ]
YieldReaction ConditionsOperation in experiment
> 95% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; 4-methyl-morpholine; 1-methyl-pyrrolidin-2-one; at 20℃; for 18h; A solution of 2,5-dihydro-pyrrole-l,2-dicarboxylic acid 1-tert-butyl ester (392.4 mg, 1.84 mmol) and (R)-1, 2,3, 4-tetrahydro-naphthalen-l-ylamine (564.3 mg, 3.83 mmol) in teti-ahydrofuran (THF) (40 niL) was added l-ethyl-3-(3- dimethylaminopropyl)carbodiimide hydrocliloride (EDCI) (860 mg, 4.48 mmol) and 1- hydroxybenzotriazole monohydrate (HOBt) (450 mg, 3.33 mmol), followed by JV-methyl- 2-pyrrolidinone (0.75 mL) and 4-methyl morpholine (0.75 mL). This mixture was stirred at room temperature for 18 hours. The reaction mixture was treated with water (20 mL), then partitioned between ethyl acetate/water. The organic phase was washed with IN HCl (2 x 25 mL), saturated sodium bicarbonate solution (50 mL) and brine solution (50 mL), dried over Na2SO4 and evaporated to dryness. The residue was purified by medium pressure column chromatography on silica gel eluting with ethyl acetate/hexane (0-100%) to give the title compound (630 mg, >95%) as a glassine solid. TLC (50% ethyl acetate/hexane) R7= 0.31; MS (ES) for C20H26N2O3 (MW=342.43): positive 343 (M+H).
 

Historical Records