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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352335Generated: October 25, 2026

1-Bromopropane → 5-Nitro-1-propylindoline

https://huagongshe.com/reaction/352335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
Reactant5-NitroindolineHCID 36219—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Nitro-1-propylindolineHCID 9834276—

Reaction Steps

0.51 g (12.79 mmoles) of 60% NaH is added, at 20° C., by portions, to a solution of 2 g (12.18 mmoles) of 5-nitroindoline in 16 ml of anhydrous DMF. After stirring for a further 30 minutes, 2.32 ml (25.58 mmoles) of 1-bromopropane is added dropwise. Stirring is maintained overnight and the reaction mixture is finally diluted with 50 ml of water and 50 ml of AcOEt. After stirring and decanting, the organic phase is successively washed with 25 ml of water and 25 ml of salt water, dried over Na2SO4, filtered and concentrated to dryness under vacuum. The evaporation residue is then purified on a silica column (eluent: Heptane/AcOEt: 9/1). Orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747024B1
Source datasetuspto-grants-2004_06
ORD IDord-796e6a3fb63845a989e31572ba112b64
Source noteuspto-grants-2004_06