ChemicalBook--->CAS DataBase List--->87932-49-8

87932-49-8

87932-49-8 Structure

87932-49-8 Structure
IdentificationBack Directory
[Name]

Nsc21187
[CAS]

87932-49-8
[Synonyms]

Nsc21187
3-chloro-4,5-dihydroxybenzoic acid
Benzoic acid, 3-chloro-4,5-dihydroxy-
[Molecular Formula]

C7H5ClO4
[MDL Number]

MFCD01742816
[MOL File]

87932-49-8.mol
[Molecular Weight]

188.57
Chemical PropertiesBack Directory
[Boiling point ]

391.7±42.0 °C(Predicted)
[density ]

1.702±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.08±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

Nsc21187(87932-49-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-CHLOROVANILLIC ACID

62936-23-6

Nsc21187

87932-49-8

General procedure for the synthesis of 3-chloro-4,5-dihydroxybenzoic acid from 3-chloro-4-hydroxy-5-methoxybenzoic acid: Step (i): tribromoborane (7.86 mL, 82 mmol) was added dropwise to a stirred solution of 3-chloro-4-hydroxy-5-methoxybenzoic acid (6.61 g, 32.6 mmol) in dichloromethane (50 mL) under nitrogen protection. The reaction mixture was continued to be stirred at 0 °C for 2 h and subsequently poured in batches into ice/brine (250 mL). The aqueous phase was extracted with ethyl acetate (2 x 150 mL) and the combined organic phases were dried over magnesium sulfate and filtered. The solvent was removed by concentration under reduced pressure to give 3-chloro-4,5-dihydroxybenzoic acid (5.11 g, 79% yield). Mass spectrum (electrospray ionization, negative mode) m/z 187 [M-H]? ; 1H NMR (400 MHz, DMSO-d?) δ: 12.69 (1H, broad single peak), 10.14 (2H, broad single peak), 7.35 (1H, double peak), 7.32 (1H, double peak).

[References]

[1] Patent: WO2011/27106, 2011, A1. Location in patent: Page/Page column 106-107
[2] Patent: US2012/149737, 2012, A1. Location in patent: Page/Page column 58
[3] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 4, p. 798 - 814
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