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16694-17-0

16694-17-0 Structure

16694-17-0 Structure
IdentificationBack Directory
[Name]

4-BROMOTHIOPHENE-3-CARBOXYLIC ACID
[CAS]

16694-17-0
[Synonyms]

Einecs 240-739-8
4-bromo-3-thenoic acid
4-Bromo-3-carboxythiophene
4-Bromothiophenecarboxylicacid
4-Bromo-3-thiophenecarboxylicacid
4-BROMOTHIOPHENE-3-CARBOXYLIC ACID
4-Bromothiophene-3-carvoxylic acid
3-Bromo-4-thiophenecarboxylic acid
3-Thiophenecarboxylic acid, 4-broMo-
4-Bromo-3-thiophenecarboxylic acid 97%
3-Bromo-4-carboxythiophene, 4-Bromo-3-thenoic acid
4-BROMOTHIOPHENE-3-CARBOXYLIC ACID ISO 9001:2015 REACH
[hydroxy-[[(2R,3S,5R)-3-hydroxy-5-[5-(hydroxymethyl)-2,4-dioxo-1-pyrimidinyl]-2-oxolanyl]methoxy]phosphoryl] phosphono hydrogen phosphate
[EINECS(EC#)]

240-739-8
[Molecular Formula]

C5H3BrO2S
[MDL Number]

MFCD01233020
[MOL File]

16694-17-0.mol
[Molecular Weight]

207.05
Chemical PropertiesBack Directory
[Melting point ]

157-159℃
[Boiling point ]

318.0±27.0 °C(Predicted)
[density ]

1.923±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

3.63±0.20(Predicted)
[color ]

Off-white/faint brown
[InChI]

InChI=1S/C5H3BrO2S/c6-4-2-9-1-3(4)5(7)8/h1-2H,(H,7,8)
[InChIKey]

APBIZVFQQBCAAT-UHFFFAOYSA-N
[SMILES]

C1SC=C(Br)C=1C(O)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501
[Hazard Codes ]

Xi
[WGK Germany ]

2
[Hazard Note ]

Irritant
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMOTHIOPHENE-3-CARBOXYLIC ACID(16694-17-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,4-Dibromothiophene

3141-26-2

Carbon dioxide

124-38-9

4-BROMOTHIOPHENE-3-CARBOXYLIC ACID

16694-17-0

Cool 100 mL of ether to -78°C under a nitrogen atmosphere. A 1.6 M n-butyllithium solution (28.4 mL) was slowly added. Subsequently, a solution of 3,4-dibromothiophene (10 g, 41.3 mmol) dissolved in 50 mL of ether was added dropwise over 10 min. The reaction temperature was maintained at -78 °C and stirring was continued for 10 min before an excess (>50 g) of fresh powdered dry ice (CO?) was added. The reaction mixture was stirred at -78°C for 1 hour, then 30 mL of 1 M NaOH solution (pre-diluted with 100 mL of water) was slowly added (note: CO? will be released). Gradually increase the temperature until the ice melts. Separate the organic and aqueous phases and extract the ether phase with 25 mL of 1 N NaOH solution. Combine all aqueous phases and acidify with 100 mL of 1 N HCl solution to pH < 7. Collect the precipitated white precipitate by filtration, wash with water, and dry in a vacuum oven to give 4-bromothiophene-3-carboxylic acid as a white solid (5.8 g, 68% yield).

[References]

[1] Pharmazie, 2006, vol. 61, # 11, p. 901 - 907
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1994, # 19, p. 2735 - 2744
[3] Patent: WO2006/3096, 2006, A1. Location in patent: Page/Page column 71-72
[4] Patent: US2013/116233, 2013, A1. Location in patent: Paragraph 1018; 1019
[5] Patent: WO2014/140086, 2014, A1. Location in patent: Page/Page column 68-69
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