HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430879Generated: October 29, 2026
Toluene → Diethyl 2-(4'-hexyloxyphenyl)terephthalate
https://huagongshe.com/reaction/430879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hexyloxyphenylboronic Acid | HCID 3682148 | — |
| Reactant | Diethyl 2-bromoterephthalate | HCID 11033938 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diethyl 2-(4'-hexyloxyphenyl)terephthalate | HCID 11069361 | — |
Reaction Steps
Diethyl bromoterephthalate (30.1 g, 100 mmol), K2CO3 (27.6 g, 200 mmol) and 140 ml of toluene and 140 ml of H2O were placed in a reaction vessel and argon was passed in for 30 minutes. 4-hexyloxyphenylboronic acid (26.7 g, 120 mmol) (cf. B1) and Pd(PPh3)4 (1.16 g, 1 mmol) were subsequently added under protective gas. The yellow-green, turbid mixture was stirred vigorously under a blanket of protective gas at an internal temperature of 85° C. After 7 hours, the reaction wag complete. After phase separation, the organic phase was shaken with dilute HCl/H2O (until neutral). The aqueous phase was shaken with toluene and the organic phases were combined. After filtering off any palladium residues, the solution was evaporated. The product was obtained as a yellowish brown oil in sufficient purity (about 86%): 44.7 g (1112%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323373B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-307ef639c86d4e6cb67260fadae421f0 |
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| Source note | uspto-grants-2001_11 |
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