Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466314Generated: November 2, 2026

Hydrazine hydrate (1:1) → 1,3-Dihydro-5-methoxy-1-(phenylmethyl)-2H-indol-2-one

https://huagongshe.com/reaction/1466314

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 H2SO04, 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 [C16H15NO2+H]+ 254.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999968B2
Source datasetuspto-grants-2015_04
ORD IDord-f08d8a9cabd04cefb0b1362b485e4132
Source noteuspto-grants-2015_04