Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082503Generated: October 31, 2026

Benzoyl chloride → HCID 21460685, compound

https://huagongshe.com/reaction/2082503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21460705HCID 21460705—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21460685HCID 21460685—

Reaction Steps

Suspend the 3-amino-2-carbethoxy-6-nitroindole (0.6 mmol) in tetrahydrofuran (mL) and add triethylamine (0.62 mmol). Add benzoyl chloride (0.62 mmol) and stir for 30 minutes at room temperature. Dilute the reaction with ethyl acetate, 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-nitroindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189054
Source datasetuspto-grants-1993_02
ORD IDord-3d8153e6ddb346748b58556ccbc2621e
Source noteuspto-grants-1993_02