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(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID

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(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Basic information

Product Name:
(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
Synonyms:
  • (R)-(-)-GAMMA-CARBOXY-GAMMA-BUTYROLACTONE
  • (R)-GAMMA-CARBOXY-GAMMA-BUTYROLACTONE
  • (R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
  • (R)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
  • (R)-(-)-5-OXO-2-TETRAHYDROFURANCARBOXYLIC ACID
  • (R)-(-)-5-OXO-2-TETRAHYDROFUROIC ACID
  • (R)-(-)-TETRAHYDRO-5-OXO-2-FURANECARBOXYLIC ACID
  • (R)-(-)-5-OXO-2-TETRAHYDROFURANCARBOXYLI C ACID, 98% (97% EE/GLC)
CAS:
53558-93-3
MF:
C5H6O4
MW:
130.1
Product Categories:
  • Carboxylic Acids (Chiral)
  • Chiral Building Blocks
  • Synthetic Organic Chemistry
Mol File:
53558-93-3.mol
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(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Chemical Properties

Melting point:
71-73 °C (lit.)
Boiling point:
165-167 °C/0.3 mmHg (lit.)
alpha 
-14°(D/20℃) (c=5, メタノール)
Density 
1.3985 (rough estimate)
refractive index 
1.5800 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
pka
3.11±0.20(Predicted)
Appearance
White to light yellow Solid
optical activity
[α]20/D 14°, c = 5 in methanol
BRN 
1424499
InChI
InChI=1S/C5H6O4/c6-4-2-1-3(9-4)5(7)8/h3H,1-2H2,(H,7,8)/t3-/m1/s1
InChIKey
QVADRSWDTZDDGR-GSVOUGTGSA-N
SMILES
O1C(=O)CC[C@@H]1C(O)=O
CAS DataBase Reference
53558-93-3(CAS DataBase Reference)
EPA Substance Registry System
2-Furancarboxylic acid, tetrahydro-5-oxo-, (2R)- (53558-93-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29321900

MSDS

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(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

(R)-5-Oxotetrahydrofuran-2-carboxylic Acid is an intermediate used to synthesize 2'',3''-dideoxy-4''-selenonucleosides as potential antiviral agents.

General Description

(R)-(?)-5-Oxo-2-tetrahydrofurancarboxylic acid belongs to the class of furans, considered as heterocyclic building blocks. It is used as an HPLC derivatization reagent for UV/Vis detection.

Synthesis

6893-26-1

53558-93-3

Example 1: Synthesis of (R)-(-)-5-oxo-2-tetrahydrofuran carboxylic acid (2) 1. To a mixed solution of D-glutamic acid (1 , 25 g, 170 mmol) in water (67 mL) and concentrated hydrochloric acid (35 mL) was slowly added a solution of NaNO2 (17.5 g, 253.6 mmol) in water (37.5 mL) at 0 °C for 4 hours. 2. After the addition was completed, the reaction mixture was stirred overnight at room temperature to obtain a clarified solution. 3. The solvent was removed by vacuum evaporation and the residue was treated with ethyl acetate (EtOAc, 80 mL) and filtered. 4. The filtrate was dried over anhydrous sodium sulfate (Na2SO4) and subsequently concentrated. 5. The concentrated residue was crystallized from a solvent mixture of ethyl acetate/benzene/hexane to afford (R)-(-)-5-oxo-2-tetrahydrofuran carboxylic acid (2) as a white crystalline solid (12.63 g, 57% yield). Product Characterization: - Melting point: 71-73°C - 1H NMR (400 MHz, CD3OD): δ 4.20 (m, 1H, CHO), 1.8-2.3 (m, 4H, CH2CH2).

References

[1] Tetrahedron, 2006, vol. 62, # 37, p. 8687 - 8695
[2] Tetrahedron: Asymmetry, 1993, vol. 4, # 6, p. 1391 - 1396
[3] Organic Letters, 2014, vol. 16, # 16, p. 4336 - 4339
[4] Pharmazie, 1995, vol. 50, # 1, p. 15 - 21
[5] Patent: US2004/67877, 2004, A1

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