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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl vinyl etherHCID 8108—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-1-iodo-2-methoxybenzeneHCID 16079230—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventDimethylformamideHCID 6228—
Product1-(4-Chloro-2-methoxyphenyl)ethan-1-oneHCID 1942946865%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456169B2
Source datasetuspto-grants-2008_11
ORD IDord-e8602a0c38a644c68b43f7f62fb8f50e
Source noteuspto-grants-2008_11