HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965231Generated: October 27, 2026
Sodium hydride → 4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dione
https://huagongshe.com/reaction/1965231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloroisatin | HCID 96047 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dione | HCID 67356554 | 81.7% |
Reaction Steps
To a stirred solution of 4-chloroisatin (9.10 g, 50.0 mmol) in N,N-dimethylformamide (100 mL) was added sodium hydride (2.20 g, 55.0 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 1 h, followed by the addition of bromodiphenylmethane (14.80 g, 56.8 mmol). The mixture was stirred at ambient temperature for 20 h, diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was recrystallized from diethyl ether and hexanes to afford 4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dione (14.20 g, 81%): 1H NMR (300 MHz, CDCl3) 7.37-7.17 (m, 11H), 6.98-6.95 (m, 2H), 6.42 (d, J=9.0 Hz, 1H); MS (ES+) m/z 369.9 (M+23), 371.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415370B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-eb907f66c9ab4d0192518a9d8c3ae046 |
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| Source note | uspto-grants-2013_04 |
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