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70829-28-6

70829-28-6 Structure

70829-28-6 Structure
IdentificationBack Directory
[Name]

3-Cyano-4-hydroxybenzoic acid
[CAS]

70829-28-6
[Synonyms]

3-Cyano-4-hydroxybenzoicaci
3-Cyano-4-hydroxybenzoic acid
Benzoic acid, 3-cyano-4-hydroxy-
3-Cyano-4-hydroxybenzoic acid 95+%
5-Carboxy-2-hydroxybenzonitrile, 4-Carboxy-2-cyanophenol
[Molecular Formula]

C8H5NO3
[MDL Number]

MFCD09998350
[MOL File]

70829-28-6.mol
[Molecular Weight]

163.13
Chemical PropertiesBack Directory
[Melting point ]

265-266 °C
[Boiling point ]

392.4±37.0 °C(Predicted)
[density ]

1.50±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

4.01±0.10(Predicted)
[color ]

Off-white to faint yellow
[InChI]

InChI=1S/C8H5NO3/c9-4-6-3-5(8(11)12)1-2-7(6)10/h1-3,10H,(H,11,12)
[InChIKey]

KUCSFDLSLAVLBY-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=C(O)C(C#N)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2918290090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-Iodo-4-propoxybenzoic acid-->methyl 3-cyano-4-hydroxybenzoate-->METHYL 3-CYANO-4-METHOXYBENZOATE-->METHYL 4-HYDROXY-3-IODOBENZOATE-->sodium:cyanide
Spectrum DetailBack Directory
[Spectrum Detail]

3-Cyano-4-hydroxybenzoic acid(70829-28-6)1HNMR
3-Cyano-4-hydroxybenzoic acid(70829-28-6)FT-IR
Hazard InformationBack Directory
[Synthesis]

sodium:cyanide

773837-37-9

3-Iodo-4-propoxybenzoic acid

1131588-12-9

3-Cyano-4-hydroxybenzoic acid

70829-28-6

General procedure for the synthesis of 3-carbonitrile-4-hydroxybenzoic acid from compound (CAS: 773837-37-9) and compound (CAS: 1131588-12-9): the product of Example 44 Step C (0.22 g, 0.72 mmol), NaCN (0.04 g, 0.8 mmol), and CuCN (0.07 g, 0.8 mmol) in anhydrous DMF (2 mL) was stirred at 110 °C for 2 h in a nitrogen atmosphere. Upon completion of the reaction, the mixture was evaporated to dryness under vacuum and the residue was suspended in water (10 mL) and the pH was adjusted with 1 M NaOH solution to about 10. The insoluble material was removed by filtration and the filtrate was acidified with dilute HCl to pH ~3. The product was extracted with dichloromethane (2 x 20 mL). The organic phases were combined and dried with anhydrous MgSO4, and the filtrate was filtered and evaporated to dryness under reduced pressure to give 3-carbonitrile-4-hydroxybenzoic acid (0.1 g, 67% yield) as a brown solid.1H-NMR (CDCl3) δ: 1.06-1.14 (m, 3H), 1.85-1.97 (m, 2H), 4.1-4.18 (m, 2H), 7.02 (d , 1H, J = 9 Hz), 8.24 (dd, 1H, J = 3, 9 Hz), 8.31 (d, 1H, J = 3 Hz).

[References]

[1] Patent: WO2010/42998, 2010, A1. Location in patent: Page/Page column 109
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