HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537683Generated: October 25, 2026
1,2-Dimethoxyethane → 9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione
https://huagongshe.com/reaction/537683
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Iodine, ion (I1+) | HCID 3715291 | — |
| Reactant | 2-Ethyl-5-bromophenylboronic acid | HCID 59445941 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione | HCID 66679999 | — |
Reaction Steps
A portion of the iodonium ylide (2.0 g, 5.21 mmol) is added to a mixture of 2-ethyl-5-bromophenylboronic acid (1.43 g, 6.25 mmol), palladium(II) acetate (59 mg, 0.26 mmol) and lithium hydroxide monohydrate (0.656 g, 15.6 mmol) in 1,2-dimethoxyethane (40 ml) and water (10 ml), and the mixture is heated at 50° C. for 6 hours, and then allowed to stand at room temperature overnight. The mixture is filtered through diatomaceous earth, washing the filter cake with water (50 ml) and ethyl acetate (50 ml). The organic phase is discarded. The aqueous phase is acidified to pH2 by addition of concentrated hydrochloric acid, and then extracted with ethyl acetate. The organic extract is dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 9-(5-bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865623B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-145deb73b74741cb952ea9c9df55a26f |
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| Source note | uspto-grants-2014_10 |
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