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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396338Generated: November 2, 2026

Benzoyl chloride → HCID 21460729, compound

https://huagongshe.com/reaction/2396338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21460740HCID 21460740—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21460729HCID 2146072956%

Reaction Steps

Suspend the 3-amino-2-carbethoxy-6-trifluoromethylindole (290 mg, 1.06 mmol) in tetrahydrofuran (30 mL) and add triethylamine (0.150 mL, 1.17 mmol). Add benzoyl chloride (0.136 mL, 1.17 mmol) and stir for 30 minutes at room temperature. Dilute the reaction with ethyl acetate (mL), rinse with 1M HCl, water, dry over magnesium sulfate, filter and concentrate in vacuo. Recrystallize from hot ethyl acetate/hexane to yield 3-[(phenacyl)amino]-2-carbethoxy-6-trifluoromethylindole (230 mg, 56%); mp237°-239° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491153
Source datasetuspto-grants-1996_02
ORD IDord-f9ddd2c83cfe48c39282d4d43659bd83
Source noteuspto-grants-1996_02