HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884210Generated: October 26, 2026
Sulfuric Acid → 158938-08-0 4-N-Pentoxyterphenyl-carbonic acid
https://huagongshe.com/reaction/1884210
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4'-Iodobiphenyl-4-carboxylic acid | HCID 816730 | — |
| Reactant | 4-Pentyloxyphenylboronic Acid (contains varying amounts of Anhydride) | HCID 4684888 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Water | HCID 962 | — |
| Product | 158938-08-0 4-N-Pentoxyterphenyl-carbonic acid | HCID 9798987 | — |
Reaction Steps
162 g of 4′-iodobiphenyl-4-carboxylic acid are introduced together with 129 g of glycol ester of 4-n-pentoxyphenylboronic acid and 79.5 g of sodium carbonate into 1.5 l of ethylene glycol and, while stirring vigorously, 17.5 ml of a Pd(dba)2 solution are added and the mixture is stirred at 80° C. for 6 hours. The hot reaction mixture is cautiously poured into a mixture of 150 g of 37% strength sulfuric acid and 1,000 g of water, and the mixture is heated at 90-100° C. for 30 minutes. After filtration and washing with water, the crude product is dried at 80° C./100 mbar and then recrystallized from dimethylacetamide. This affords after drying 132 g (73%) of 4″-n-pentoxyterphenyl-4-carboxylic acid with a purity of >99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762315B1 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-ef422a8eb7bc48e5bf6b9506e63bebb0 |
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| Source note | uspto-grants-2004_07 |
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