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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488622Generated: October 25, 2026

Isopropenyl acetate → 1-(1-methyl-1H-indol-4-yl)propan-2-one

https://huagongshe.com/reaction/488622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantMethoxytri-n-butylstannaneHCID 11964040—
Reactant4-Chloro-1-methyl-1H-indoleHCID 13048759—
SolventTolueneHCID 1140—
Product1-(1-methyl-1H-indol-4-yl)propan-2-oneHCID 22270477—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 0.852 g (5.14 mmol) of 4-chloro-1-methylindole in 15 mL dry toluene, 0.85 mL (7.73 mmol) isopropenyl acetate and 2.3 mL (8 mmol) tributyltin methoxide were added. The solution was heated to 100° C. After 15 min 0.24 g (0.61 mmol) 2-dicyclohexylphospino-2′-(N,N-dimethylamino)biphenyl and 0.14 g (0.153 mmol) tris(dibenzylidineacetone)dipalladium were added and heating was continued. After 2 h the solution was cooled, filtered through a pad of CELITE diatomaceous earth and the filtrate was concentrated to ca. 5 mL. This solution was purified on a silica column using a gradient of 5-20% EtOAc/hexane to obtain the title compound. 1H NMR: (500 MHz, CDCl3): δ 2.14 (s, 3H), 3.84 (s, 3H), 3.97 (s, 2H), 6.51 (d, 1H), 7-7.3 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972295B2
Source datasetuspto-grants-2005_12
ORD IDord-c1632b9b5df64b979cf8905f7b3a1df2
Source noteuspto-grants-2005_12