HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970832Generated: October 27, 2026
Water → 4-Allyl-1-ethoxymethoxy-2-ethylbenzene
https://huagongshe.com/reaction/970832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | 4-Bromo-1-ethoxymethoxy-2-ethylbenzene | HCID 17983114 | — |
| Catalyst | HCID 178479802 | HCID 178479802 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Allyl-1-ethoxymethoxy-2-ethylbenzene | HCID 17983047 | — |
Reaction Steps
15 g (58 mmol) of 4-bromo-1-ethoxymethoxy-2-ethylbenzene are dissolved in 150 ml of DMF. 26.9 ml (87 mmol) of allyltributyltin are added, and then the mixture is degassed with a nitrogen stream. 1.2 g (1.8 mmol) of dichlorobis (triphenylphosphino)palladium are added, and the medium is heated at 120° C. for 10 hours. The reaction medium is poured into water, and then extracted with ethyl acetate. The residue obtained after drying and concentration is purified by chromatography on a silica column (eluent heptane, and then heptane 95/ethyl acetate 5). A yellow oil is obtained (m=13.6 g, y=100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312249B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-d5e7f628861b4b65825e5f028e8db75f |
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| Source note | uspto-grants-2007_12 |
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