HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24794Generated: October 26, 2026
N-Methyloxindole → HCID 178481538, compound
https://huagongshe.com/reaction/24794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyloxindole | HCID 6096 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178481538 | HCID 178481538 | — |
Reaction Steps
4.15 g (41 mmol) of diisopropylamine are placed in 50 ml of THF, cooled to −70° C. and combined with a solution of 14.4 ml of (36 mmol) of n-butyl lithium solution (2.5 mol in toluene) and stirred for 10 minutes. Then a solution of 5.0 g (34 mmol) of 1-methyl-2-indolinone in 30 ml of THF is added dropwise and stirred for 45 minutes at −70° C. Then 5.8 g (0.041 mol) of benzoylchloride are added dropwise. The reaction solution is left to heat up slowly within 14 hours. It is then poured onto sodium chloride solution and extracted with ethyl acetate. The combined organic extracts are dried and concentrated by evaporation. The residue is chromatographed on silica gel (dichloromethane/methanol/ammonia=200:8:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855710B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-a1c7c69415544c0fba466205d97cb0f2 |
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| Source note | uspto-grants-2005_02 |
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