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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527444Generated: October 25, 2026

Water → methyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetate

https://huagongshe.com/reaction/527444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 2-(5-methoxy-1H-indol-3-yl)acetateHCID 594955—
SolventDimethylformamideHCID 6228—
Productmethyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetateHCID 57563309—

Reaction Steps

Methyl 2-(5-methoxy-1H-indol-3-yl)acetate (60 mg, 0.27 mmol) and NaH (8 mg, 0.33 mmol) were stirred in anhydrous DMF (1 mL) at 0° C. under argon for 30 min, at which time 4-chlorobenzoyl chloride (57 mg, 0.33 mmol) was added. The reaction mixture was stirred overnight at room temperature and was then poured into cold water (2 mL). The organic compound was immediately extracted with dichloromethane (2×2 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified on silica (ethyl acetate/hexane gradient) and recrystallized from hexane. Yield: 18 mg (18%). C19H16ClNO4, Mr=357.79; 1H NMR (400 MHz, DMSO-d6) d: 3.61 (s, 3H), 3.78 (s, 2H), 3.81 (s, 3H), 7.00 (dd, J=2.4/9.0 Hz, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.35 (s, 1H), 7.65-7.77 (m, 4H), 8.17 (d, J=8.8 Hz, 1H); LCMS (ESI) tR: 2.81 min (>99%, ELSD), m/z: 358.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346803B2
Source datasetuspto-grants-2016_05
ORD IDord-64547cd1dbe042d9896b7a22cb3b889b
Source noteuspto-grants-2016_05