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4-Bromo-benzo[b]thiophene-2-carboxylic acid

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4-Bromo-benzo[b]thiophene-2-carboxylic acid manufacturers

4-Bromo-benzo[b]thiophene-2-carboxylic acid Basic information
Product Name:4-Bromo-benzo[b]thiophene-2-carboxylic acid
Synonyms:Benzo[b]thiophene-2-carboxylic acid, 4-bromo-;4-Bromobenzothiophene-2-carboxylic acid;4-Bromobenzo[b]thiophene-2-carboxylicaci;4-BROMO-1-BENZOTHIOPHENE-2-CARBOXYLIC ACID;4-Bromo-benzo[b]thiophene-2-carboxylic acid
CAS:5194-37-6
MF:C9H5BrO2S
MW:257.1
EINECS:1592732-453-0
Product Categories:
Mol File:5194-37-6.mol
4-Bromo-benzo[b]thiophene-2-carboxylic acid Structure
4-Bromo-benzo[b]thiophene-2-carboxylic acid Chemical Properties
Melting point 265
Boiling point 429.7±25.0 °C(Predicted)
density 1.813±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
form powder
pka3.27±0.30(Predicted)
color White
InChIInChI=1S/C9H5BrO2S/c10-6-2-1-3-7-5(6)4-8(13-7)9(11)12/h1-4H,(H,11,12)
InChIKeyLAYNZUFIYSYHIV-UHFFFAOYSA-N
SMILESC12=CC=CC(Br)=C1C=C(C(O)=O)S2
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 2934999090
MSDS Information
4-Bromo-benzo[b]thiophene-2-carboxylic acid Usage And Synthesis
Uses4-BROMO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID can be used as a key intermediate in the synthesis of pharmaceuticals. It has potentially biological activity.
Synthesis
Ethyl 4-broMo-1-benzothiophene-2-carboxylate

93103-82-3

4-BROMO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID

5194-37-6

Step 3: (0367) To a 500 mL single neck flask was added ethyl 4-bromo-1-benzothiophene-2-carboxylate (20 g, 70.4 mmol), tetrahydrofuran (120 mL) and water (100 mL). Aqueous 4 N sodium hydroxide (40 mL) was added slowly with stirring, followed by heating the reaction mixture to 70 °C with continuous stirring for 1 hour. After completion of the reaction, the reaction mixture was extracted with ethyl acetate (70 mL x 2). The pH of the aqueous phase was adjusted to 12 with concentrated hydrochloric acid and the precipitated solid was filtered and dried to give 4-bromobenzo[b]thiophene-2-carboxylic acid (16 g, yield: 88%).

References[1] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1984, vol. 23, # 1, p. 38 - 41
[2] Patent: US2017/158680, 2017, A1. Location in patent: Paragraph 0361; 0366; 0367
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