HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160723Generated: October 26, 2026
Isopropenyl acetate → 1-(1-methyl-1H-indol-4-yl)propan-2-one
https://huagongshe.com/reaction/1160723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | Methoxytri-n-butylstannane | HCID 11964040 | — |
| Reactant | 4-Chloro-1-methyl-1H-indole | HCID 13048759 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(1-methyl-1H-indol-4-yl)propan-2-one | HCID 22270477 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816534B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-4e02c747dbb0436a80db8facd1e08965 |
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| Source note | uspto-grants-2010_10 |
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