HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447352Generated: October 26, 2026
Hydrazine hydrate (1:1) → 1,3-Dihydro-5-methoxy-1-(phenylmethyl)-2H-indol-2-one
https://huagongshe.com/reaction/447352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-Benzyl-5-methoxyisatin | HCID 11357627 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,3-Dihydro-5-methoxy-1-(phenylmethyl)-2H-indol-2-one | HCID 11357226 | 85.8% |
Reaction Steps
A solution of 1-benzyl-5-methoxyindoline-2,3-dione (6.1 g, 23 mmol) and hydrazine hydrate (50-60% grade, 2.9 mL, ca. 2 eq) in DMSO (15 mL) is heated to 140° C. in an oil bath. After 3 h, the mixture was cooled, diluted with water and EtOAc, the layers separated and the aqueous extracted with EtOAc three times (30 mL). The combined organic portions were washed with 2M H2SO4, brine, and dried over MgSO4, filtered and concentrated to afford the crude product as a viscous brown oil. The crude product was purified by silica gel chromatography (20-50% EtOAc in hexane) to yield the title compound as a brown oil (5.0 g, 85%). 1H NMR (400 MHz, CDCl3) δ 7.34-7.23 (m, 5H), 6.89 (s, 1H), 6.69 (d, J=8.3 Hz, 1H), 6.61 (d, J=8.5 Hz, 1H), 4.91 (s, 2H), 3.76 (s, 3H), 3.62 (s, 2H). MS ESI 254.0 [M+H]+, calcd for [C16H1sNO2+H]+ 254.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481533B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-077e2fe138f048c6b49a45ec57f07c34 |
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| Source note | uspto-grants-2013_07 |
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