HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229716Generated: October 26, 2026
1-Dodecyne → 5-(Dodec-1-YN-1-YL)-2-hydroxybenzene-1,3-dicarbaldehyde
https://huagongshe.com/reaction/229716
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Dodecyne | HCID 69821 | — |
| Reactant | 5-Bromo-2-hydroxybenzene-1,3-dicarbaldehyde | HCID 5260206 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(Dodec-1-YN-1-YL)-2-hydroxybenzene-1,3-dicarbaldehyde | HCID 59710865 | 46% |
Reaction Steps
2,6-Diformyl-4-bromophenol (2.50 g, 10.9 mmol), 1-dodecyne (2.00 g, 12.0 mmol), Cul (65 mg, 0.33 mmol), and bis(triphenylphosphine)palladium)II)dichloride were suspended in degassed acetonitrile (MeCN) (5 mL) and degassed benzene (1 mL). The yellow suspension was sparged with argon for 30 min and degassed Et3N (1 mL) was added. The resulting brown suspension was sealed in a pressure vial, warmed to 80° C. and held there for 12 h. The mixture was then partitioned between EtOAc and KHSO4 solution. The organic layer was separated, washed with brine, dried MgSO4) and concentrated under reduced pressure. The dark yellow oil was purified by column chromatography on silica gel (25% Et2O in hexanes) to give 1.56 g (46%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563890B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-2fe543425c5d41608322a71ab1ccb910 |
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| Source note | uspto-grants-2009_07 |
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