Home Cart Sign in  
Chemical Structure| 86954-05-4 Chemical Structure| 86954-05-4

Structure of 86954-05-4

Chemical Structure| 86954-05-4

*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 [ 86954-05-4 ]

CAS No. :86954-05-4
Formula : C13H17NO3
M.W : 235.28
SMILES Code : O=C(N1C(CO)CCC1)OCC2=CC=CC=C2
MDL No. :MFCD09953280
InChI Key :BJTNHGVCFWDNDP-UHFFFAOYSA-N
Pubchem ID :4576020

Safety of [ 86954-05-4 ]

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

Application In Synthesis of [ 86954-05-4 ]

* 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 [ 86954-05-4 ]

[ 86954-05-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 112380-58-2 ]
  • [ 498-63-5 ]
  • [ 86954-05-4 ]
  • 2
  • [ 501-53-1 ]
  • [ 498-63-5 ]
  • [ 86954-05-4 ]
YieldReaction ConditionsOperation in experiment
With dmap; In tetrahydrofuran; at 20℃; for 10h; The starting material of the intermediate 1 was dissolved in tetrahydrofuran, 4-dimethylaminopyridine was added, and benzyl chloroformate was added in portions, and the reaction was carried out for 10 hours at room temperature.The progress of the reaction was checked by TLC, the reaction was quenched, water and dichloromethane were extracted, and the organic phase was washed with acid and alkali, respectively.Concentration, separation and purification by column chromatography to obtain intermediate 2,
  • 3
  • [ 1885-14-9 ]
  • [ 498-63-5 ]
  • [ 86954-05-4 ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate; In dichloromethane; Step A: 1-Benzyloxycarbonyl-2-pyrrolidinemethanol 2-Pyrrolidinemethanol (2 g, 20 mmol) was dissolved in CH2Cl2 (25 mL) followed by addition of saturated NaHCO3 (25 mL). To this vigorously stirred mixture was added benzylchloroformate via syringe slowly at 0° C. The reaction mixture was then stirred at room temperature for 4 h. The organic layer was separated and the aqueous layer was extracted with CH2Cl2 (3*80 mL). The combined organic layer was washed with brine, and dried (Na2SO4). Removal of the solvent provided 4.7 g of the title compound, which was used, directly for next step. 1H NMR (CDCl3): delta 7.50-7.30 (aromatic Hs, 5H); 5.17 (s, 2H); 4.04 (brs, 1H); 3.66 (m, 2H); 3.57 (m, 1H); 3.42 (m, 1H); 2.04 (m, 1H); 1.89 (m, 1H); 1.83 (m, 1H); 1.62 (m, 1H).
 

Historical Records

Technical Information

Categories