Identification | More | [Name]
(S)-(-)-1,2,3,4-Tetrahedro-naphthoic acid | [CAS]
85977-52-2 | [Synonyms]
(s)-(-)-1,2,3,4-tetrahedro-naphthoic acid (S)-1,2,3,4-TETRAHYDRO-NAPHTHALENE-1-CARBOXYLIC ACID (S)-(-)-1,2,3,4-TETRAHYDRONAPHTHOIC ACID (S)-1,2,3,4-TETRAHYDRO-NAPHTHOIC ACID (S)-1,2,3,4-tetrahydro-1-naphthoic acid (S)-(-)-1,2,3,4-Tetrahedro-1-NaphthoicAcid (S)-1,2,3,4-TETRAHUDRO-1-NAPHTHOIC ACID (S)-1,2,3,4-tetrahydro-1-naphtoic Acid | [Molecular Formula]
C11H12O2 | [MDL Number]
MFCD07368365 | [Molecular Weight]
176.21 | [MOL File]
85977-52-2.mol |
Chemical Properties | Back Directory | [Melting point ]
54-56°C | [Boiling point ]
54-56°C | [density ]
1.186±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform | [form ]
Solid | [pka]
4.28±0.20(Predicted) | [color ]
White | [InChI]
InChI=1S/C11H12O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7H2,(H,12,13)/t10-/m0/s1 | [InChIKey]
VDLWTJCSPSUGOA-JTQLQIEISA-N | [SMILES]
[C@@H]1(C(O)=O)C2=C(C=CC=C2)CCC1 | [CAS DataBase Reference]
85977-52-2(CAS DataBase Reference) |
Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Intermediate in the preparation of Dipeptidyl Boronate Proteasome Inhibitors. | [Synthesis]
General procedure for the synthesis of (S)-tetrahydronaphthalenecarboxylic acid from 1,2,3,4-tetrahydro-1-naphthalenecarboxylic acid: 15.6 g (0.1 mol) of 1,2,3,4-tetrahydronaphthalenecarboxylic acid and 29.8 g (0.1 mol) of quinine were added to 158 mL of a 50% (v/v) aqueous ethanol solution, and stirred for 30 min at 50 °C until complete dissolution. The progress of the reaction was monitored by thin layer chromatography (TLC) with the unfolding agent ratio of petroleum ether (PE):ethyl acetate (EA) = 1:2. Upon completion of the reaction, the reaction solution was cooled to below 0 °C overnight to promote crystallization. Subsequent to filtration, the solid was collected and dried. The dried solid was recrystallized with 90 mL of ethanol, crystallized again at 0 °C, diafiltrated and dried. The resulting product was dissolved in a mixture of 55 mL of 1 mol/L hydrochloric acid and 100 mL of ethyl acetate in a partitioning operation. The organic phase was dried and filtered and concentrated to obtain the crude product. Finally, the crude product was recrystallized from hexane to give 7.21 g of (S)-1,2,3,4-tetrahydronaphthalenecarboxylic acid in the form of white solid in 43.6% yield. | [References]
[1] Patent: CN108084176, 2018, A. Location in patent: Paragraph 0093; 0102; 0103; 0104 [2] Arkiv foer Kemi, 1958, vol. 12, p. 161,165 [3] Patent: CN107382697, 2017, A |
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