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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380574Generated: October 31, 2026

Acetyl chloride → 1-[2-(3-Ethyl-5-methyl-1,2-oxazol-4-yl)-1H-indol-3-yl]ethan-1-one

https://huagongshe.com/reaction/1380574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-(3-Ethyl-5-methyl-1,2-oxazol-4-yl)-1H-indoleHCID 13038686—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
SolventDichloromethaneHCID 6344—
Product1-[2-(3-Ethyl-5-methyl-1,2-oxazol-4-yl)-1H-indol-3-yl]ethan-1-oneHCID 12851453—

Reaction Steps

In the alternate procedure, 41.8 grams (0.163 moles) of silver triflouromethanesulfonate is added portionwise to a solution of 33.5 grams (0.148 mole) of 2-(3-ethyl-5-methyl-4-isoxazolyl)-indole in 450 milliliters of methylene chloride. The resulting suspension is then treated by dropwise addition with 12.8 grams (0.163 moles) of acetyl chloride in 50 milliliters of methylene chloride. The temperature rises to 35° C. during the addition. After the addition is complete, the mixture is stirred at room temperature for 4 hours and then filtered. The filtrate is washed with 150 milliliters of 2N sodium hydroxide, water and 2N sodium hydroxide, then dried over anhydrous magnesium sulfate and finally evaporated in vacuo to yield an oil. The oil is crystallized from ether to give 2-(3-ethyl-5-methyl-4-isoxazolyl)-3-acetyl indole, m.p. 170°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582848
Source datasetuspto-grants-1986_04
ORD IDord-26c77f74c6f64e92b9bd3df7caa7064a
Source noteuspto-grants-1986_04