HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751488Generated: October 27, 2026
2-Dicyclohexylphosphino-2-(N,N-Dimethylamino)Biphenyl → {4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetic acid ethyl ester
https://huagongshe.com/reaction/751488
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dicyclohexylphosphino-2-(N,N-Dimethylamino)Biphenyl | HCID 66545338 | — |
| Reactant | 7-Bromo-4-[2-(tetrahydropyran-2-yloxy)ethoxy]benzofuran | HCID 69267456 | — |
| Reactant | HCID 178472539 | HCID 178472539 | — |
| Catalyst | 1,5-Diphenylpenta-1,4-dien-3-one;palladium | HCID 154270 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {4-[2-(Tetrahydropyran-2-yloxy)ethoxy]benzofur-7-yl}acetic acid ethyl ester | HCID 69268314 | 54% |
Reaction Steps
Combine 7-Bromo-4-[2-(tetrahydropyran-2-yloxy)ethoxy]benzofuran (2.598 g, 7.61 mmol), bis(dibenzylideneacetone) palladium (0.461 g, 0.802 mmol), and 2-dicyclohexylphosphino-2-(N,N-dimethylamino)biphenyl (0.308 g, 0.783 mmol) in tetrahydrofuran (15 ml) under nitrogen. Add bromo(2-ethoxy-2-oxoethyl)zinc (2 equiv.), and heat the mixture at 80° C. for 16 hours. (Knochel, P.; Honed, P.; Eds. Organozinc Reagents: A Practical Approach; Oxford University Press, Inc: London, 1999). Cool the mixture to room temperature, filter through a silica plug eluting with ethyl ether, and concentrate. Purify by flash chromatography and elute with hexane:ethyl acetate to give 1.422 g (54%) of the title compound as an oil. Mass spectrum: electrospray (m/z) 265 (M++1-85).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405305B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-2c1085d664c841a6a9ad385d0d90530c |
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| Source note | uspto-grants-2008_07 |
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