HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620553Generated: October 25, 2026
Salicylaldehyde → 2-(10-Undecynyloxy)benzaldehyde
https://huagongshe.com/reaction/620553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Undecyne, 11-bromo- | HCID 117111 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(10-Undecynyloxy)benzaldehyde | HCID 15617498 | — |
Reaction Steps
To an ice-cold solution of 11-hydroxyundecyne (10 g, 59.4 mmoles) in 400 ml of methylene chloride under argon was added in one portion carbon tetrabromide (40.5 g, 0.1224 mole). The reaction mixture was stirred at 0° C. for 5 minutes and triphenylphosphine (29.43 g, 0.1122 mole) was added. The reaction was kept at 0° C. for an additional 15 minutes and stirred at room temperature for 3 hours. The methylene chloride was removed in vacuo. The residue was treated with hexane and the combined organic extract was concentrated in vacuo. The crude product was purified by flash chromatography on silica, eluting with straight hexane, to give 7.2 g (52%) of 11-bromoundecyne as a colorless oil. Following the procedures of Examples 20 and 39(a), a mixture of salicylaldehyde, 11-bromoundecyne and potassium carbonate in dimethylformamide is reacted to furnish 2-(10-undecynyloxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820719 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-42b36ef54d034d21a8378d05ae0d03bc |
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| Source note | uspto-grants-1989_04 |
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