HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721580Generated: November 2, 2026
Boronic Acid → 3-Octyloxy-6-pyridazineboronic acid
https://huagongshe.com/reaction/1721580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 3-Chloro-6-(octyloxy)pyridazine | HCID 6409850 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Octyloxy-6-pyridazineboronic acid | HCID 22413036 | — |
Reaction Steps
17.1 g (70.6 mmol) of 3-octyloxy-6-chloropyridazine are dissolved in 100 ml of absolute THF and cooled to -78° C. under a protective gas. 47.1 ml (75.2 mmol) of 1.6 molar n-butyllithium solution in hexane are then added dropwise over the course of 30 minutes. The mixture is stirred at -78° C. for a further 30 minutes. 216 ml (215.7 mmol) of 1.0 molar ZnCl2 solution in diethyl ether are subsequently slowly added dropwise, during which the temperature must not exceed -60° C. When the addition is complete, the mixture is stirred for a further 30 minutes. The crude boronic acid is employed directly, without isolation from the solution, for the subsequent couplings.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05512207 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-000217ba6f514ea88439ed3a0ee8e135 |
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| Source note | uspto-grants-1996_04 |
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