HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599174Generated: October 26, 2026
Sodium Carbonate → Sodium 2-amino-5-bromo-3-(2-thienyl)benzenesulphonate
https://huagongshe.com/reaction/1599174
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 2-Amino-5-bromo-3-iodobenzenesulphonic acid | HCID 18919385 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Sodium 2-amino-5-bromo-3-(2-thienyl)benzenesulphonate | HCID 23687032 | — |
Reaction Steps
A mixture of 36 g (95.3 mmol) of 2-amino-5-bromo-3-iodobenzenesulphonic acid and 12.2 g (95.3 mmol) of 2-thienylboronic acid in 140 ml of 1,2-dimethoxyethane in the presence of 5.5 g of tetrakis(triphenylphosphine)palladium (0) and 30.3 g of sodium carbonate is heated at 70°-75° C. for 8.5 hours. The solvent is evaporated off under vacuum, the mixture is cooled to 0° C. and washed with water to pH=7, and the residue is then taken up in an ether/ethanol mixture (95:5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739382 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-e481560d87ec4ef79703e9a0a4a5eca8 |
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| Source note | uspto-grants-1998_04 |
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