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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-Benzyl-5-methoxyisatinHCID 11357627—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1,3-Dihydro-5-methoxy-1-(phenylmethyl)-2H-indol-2-oneHCID 1135722685.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481533B2
Source datasetuspto-grants-2013_07
ORD IDord-077e2fe138f048c6b49a45ec57f07c34
Source noteuspto-grants-2013_07