(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
(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
(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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
(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
(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACIDSupplier
- Tel
- 18993966060
- sales@techbiochem.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID(53558-93-3)Related Product Information
- 2-(2-METHOXYPHENYL)-5-OXOTETRAHYDROFURAN-3-CARBOXYLIC ACID
- (R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
- (S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
- 2,2-DIMETHYL-5-OXOTETRAHYDROFURAN-3-CARBOXYLIC ACID
- 2-Tetrahydrofuroic acid
- (1R)-(+)-CAMPHANIC ACID
- (S)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID,(S)-(+)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID,5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID
- 2-(1-Carboxyundecyl)-5-oxotetrahydrofuran-2-carboxylic acid
- (R)-(-)-GAMMA-ETHOXYCARBONYL-GAMMA-BUTYROLACTONE
- (3S)-2-(2-METHOXYPHENYL)-5-OXOTETRAHYDROFURAN-3-CARBOXYLIC ACID
- 4-METHYLENE-2-OCTYL-5-OXOTETRAHYDROFURAN-3-CARBOXYLIC ACID
- 3,4,4-Trimethyl-2-oxotetrahydrofuran-3-carboxylic acid ethyl ester
- 2-[[(4S)-4-[[Cyanoacetyl]amino]-3-oxotetrahydroisoxazol]-2-yl]-5-oxotetrahydrofuran-2-carboxylic acid sodium salt
- 2-[[(4S)-4-[[Phenyl-sodiosulfoacetyl]amino]-3-oxotetrahydroisoxazol]-2-yl]-5-oxotetrahydrofuran-2-carboxylic acid sodium salt
- D-CAMPHANIC ACID ANHYDRIDE
- CAMPHANIC ACID
- 2-[[(4S)-4-[[2-Thienylacetyl]amino]-3-oxotetrahydroisoxazol]-2-yl]-5-oxotetrahydrofuran-2-carboxylic acid sodium salt
- 2-[[(4S)-4-[[2-Pyridinylthioacetyl]amino]-3-oxotetrahydroisoxazol]-2-yl]-5-oxotetrahydrofuran-2-carboxylic acid sodium salt