HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859199Generated: October 26, 2026
Sodium hydride → 3-[1-(4-Acetoxymethyl-3-(2-(trimethylsilyl)ethoxymethoxy)benzyl)-indol-3-yl]-4-(1-methyl-indol-3-yl)furan-2,5-dione
https://huagongshe.com/reaction/1859199
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(1-Methyl-indol-3-yl)-4-(indol-3-yl)-furan-2,5-dione | HCID 14855714 | — |
| Reactant | Acetic acid 4-bromomethyl-2-(2-(trimethylsilyl)ethoxymethoxy)benzyl ester | HCID 53743209 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-[1-(4-Acetoxymethyl-3-(2-(trimethylsilyl)ethoxymethoxy)benzyl)-indol-3-yl]-4-(1-methyl-indol-3-yl)furan-2,5-dione | HCID 22123258 | — |
Reaction Steps
3-(1-Methyl-indol-3-yl)-4-(indol-3-yl)-furan-2,5-dione (2.21 g, 0.61 mmol) and sodium hydrid (55-60% dispersion in oil, 0.031 g, 0.76 mmol) were dissolved in dry dimethylformamide and stirred for 20 minutes at ambient temperature before adding acetic acid 4-bromomethyl-2-(2-(trimethylsilyl)ethoxymethoxy)benzyl ester (0.25 g, 0.64 mmol). The reaction was allowed to proceed for 20 hours before adding ethyl acetate (20 mL), water (5 mL) and saturated aqueous ammonium chloride (5 mL). The phases were separated and the aqueous phase extracted with ethyl acetate (20 mL). The combined organic phases were washed with water (2×20 mL), and dried over Na2SO4. Removal of the solvent furnished crude 3-[1-(4-acetoxymethyl-3-(2-(trimethylsilyl)ethoxymethoxy)benzyl)-indol-3-yl]-4-(1-methyl-indol-3-yl)furan-2,5-dione which was dissolved in dimethylformamide (3 mL) and ammonium hydroxide (9 mL). Heating to 75° C. in a sealed tube for four hours gave, after extraction with ethyl acetate and chromatography (ethyl acetate/heptane:60/40), 98 mg of the sub-title compound as a red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153641 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-a2afa198753a481e8b53135593224297 |
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| Source note | uspto-grants-2000_11 |
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