Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  BOC-amino acid >  Ethyl 1-Boc-3-pyrrolidinecarboxylate

Ethyl 1-Boc-3-pyrrolidinecarboxylate

Basic information Safety Supplier Related

Ethyl 1-Boc-3-pyrrolidinecarboxylate Basic information

Product Name:
Ethyl 1-Boc-3-pyrrolidinecarboxylate
Synonyms:
  • ETHYL 1-BOC-3-PYRROLIDINECARBOXYLATE
  • PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER 3-ETHYL ESTER
  • ETHYL 1-BOC-BETA-PROLINATE
  • N-Boc- 3-ethyl pyrrolidine- carboxylate
  • N-Boc-3-Pyrrolidinecaboxylic acid ethyl ester
  • 1-tert-butyl 3-ethylpyrrolidine-1,3-dicarboxylate
  • N-Boc-DL-^b-proline ethyl ester, 97%
  • N-Boc- 3-ethyl pyrrolidine-
CAS:
170844-49-2
MF:
C12H21NO4
MW:
243.3
Product Categories:
  • pharmacetical
  • Acids and Derivatives
  • Amino Acids and Derivatives
Mol File:
170844-49-2.mol
More
Less

Ethyl 1-Boc-3-pyrrolidinecarboxylate Chemical Properties

Boiling point:
305.6±35.0 °C(Predicted)
Density 
1.100±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
-2.57±0.40(Predicted)
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
170844-49-2(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090
More
Less

Ethyl 1-Boc-3-pyrrolidinecarboxylate Usage And Synthesis

Synthesis

72925-15-6

24424-99-5

170844-49-2

A dichloromethane (50 mL) solution of di-tert-butyl dicarbonate (10.30 g, 47.2 mmol) was slowly added dropwise to a dichloromethane (50 mL) solution of crude ethyl 3-pyrrolidinecarboxylate (7.12 g) at 0 °C for a controlled time of 10 min or more. The reaction mixture was gradually warmed up to room temperature over 18 h. The mixture was washed with water and saturated saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford ethyl N-Boc-3-pyrrolidinecarboxylate (10.4 g, 100% yield), which could be used for the subsequent reaction without further purification.1H NMR (CDCl3) δ: 4.14 (q, 2H), 3.27-3.69 (m , 4H), 3.02 (m, 1H), 2.07-2.16 (m, 2H), 1.46 (s, 9H), 1.27 (t, 3H).

References

[1] Patent: WO2005/49602, 2005, A1. Location in patent: Page/Page column 89; 90; 130
[2] Patent: WO2005/49605, 2005, A1. Location in patent: Page/Page column 117; 118; 158

Ethyl 1-Boc-3-pyrrolidinecarboxylateSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
ITIC MEDCHEM(SUZHOU) CO.,LTD.
Tel
0512-68323967 18015559028
Email
sales@iticmedchem.com
ChemFuture PharmaTech (Jiangsu) Ltd
Tel
5108538618
Email
suger.wang@chemfuture.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com