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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 2-(5-methoxy-1H-indol-3-yl)acetate | HCID 594955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346803B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-64547cd1dbe042d9896b7a22cb3b889b |
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| Source note | uspto-grants-2016_05 |
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