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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865168Generated: November 2, 2026

Benzoyl chloride → HCID 69037395, compound

https://huagongshe.com/reaction/1865168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl 5-nitro-1H-indole-2-carboxylateHCID 280312—
ReactantSodium BicarbonateHCID 516892—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 69037395HCID 6903739587%

Reaction Steps

Ethyl 5-nitroindole-2-carboxylate (3.1) (1.5 g, 6.41 mmol) in CH2Cl2 (30 ml) was treated with benzoyl chloride (1.19 ml, 10.26 mmol), Et3N (891 μl, 6.41 mmol) and DMAP (783 mg, 6.41 mmol). The mixture was stirred for 16 h. 10% NaHCO3 (10 ml) and CH2Cl2 (10 ml) were added and the organic layer was separated. The aqueous layer was extracted with CH2Cl2 (3×5 mL). The combined organic layers were washed with H2O (10 ml), 5% HCl (10 ml) and H2O (10 ml). The solution was dried (MgSO4) and concentrated. The 10 residue was crystalised from EtOAc/Hex 1:9 to afford 1.85 g (87%) of 3.2 as a yellow powder: 1H NMR (250 MHz, CDCl3) δ ppm 8.66 (d, 1H), 8.25 (d, 1H), 7.80 (d,1H), 7.6-7.72 (m, 3H), 7.48 (m, 3H), 4.00 (q, 2H), 1.10 (t, 3H). FABMS (NBA/NaI) m/z 339 (M+H+ expected 339)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626026B2
Source datasetuspto-grants-2009_12
ORD IDord-661be6d0132d4390a5536ab5da653f90
Source noteuspto-grants-2009_12