HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272678Generated: October 26, 2026
Butyl vinyl ether → 1-(4-Chloro-2-methoxyphenyl)ethan-1-one
https://huagongshe.com/reaction/272678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyl vinyl ether | HCID 8108 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-1-iodo-2-methoxybenzene | HCID 16079230 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Chloro-2-methoxyphenyl)ethan-1-one | HCID 19429468 | 65% |
Reaction Steps
A solution of Example 59A (2.68 g, 10 mmol) in DMF (40 mL) was treated with triethylamine (1.53 mL, 11 mmol), n-butyl vinyl ether (6.5 mL, 50 mmol), DPPF (554 mg, 1 mmol) and Pd(OAc)2 (112 mg, 0.5 mmol), purged with nitrogen, heated to 80° C. for 6 hours, cooled to room temperature, and partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were washed with water and brine, dried (MgSO4), filtered, and concentrated under vacuum. The residue was purified by flash column chromatography on silica gel with 4:1 hexanes/ethyl acetate to provide 1.20 g (65%) of the desired product. MS (ESI) m/e 185 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 7.60 (d, J=8.14 Hz, 1H), 7.27 (d, J=1.70 Hz, 1H), 7.09 (dd, J=8.31, 1.86 Hz, 1H), 3.92 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456169B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-e8602a0c38a644c68b43f7f62fb8f50e |
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| Source note | uspto-grants-2008_11 |
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