HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603060Generated: November 2, 2026
Diethyl Ether → 4-(Pyridin-3-yl)benzaldehyde
https://huagongshe.com/reaction/1603060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(Pyridin-3-yl)benzaldehyde | HCID 3693046 | — |
Reaction Steps
To a solution of n-butyllithium (16 mL of a 2.5M solution in hexane=50 mL dry diethyl ether) at -78° C. was added a solution of 3-bromopyridine (6 g in 15 mL diethyl ether) and the mixture stirred for 25 minutes. At this time trimethyl borate (4.3 mL) was added and the mixture allowed to warm to room temperature. After 1 hour the reaction was quenched by the addition of 10 mL glacial acetic acid and 60 mL water and the mixture stirred for 18 hours at room temperature. The pH of the mixture was adjusted to pH12 by the addition of 2M sodium hydroxide and extracted with diethyl ether. The aqueous layer was acidified to pH 6 by the dropwise addition of 1N hydrochloric acid and extracted with methylene chloride. The combined organics were dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with 20 mL acetonitrile:water (1:1) and filtered to give the title compound (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05985901 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-dc5d4e4dc9b04ef38a604476dd1e6569 |
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| Source note | uspto-grants-1999_11 |
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