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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234901Generated: October 25, 2026

Water → 4-cyclopentyl-7-methoxycarbonyl-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/234901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromocyclopentaneHCID 8728—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-7-carboxylateHCID 10798997—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-cyclopentyl-7-methoxycarbonyl-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 2335316751.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 7-methoxycarbonyl-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (prepared in Preparation 1) (4.0 g) in dimethylformamide (80 ml) were added 60% sodium hydride (in oil) (0.73 g) and cyclopentyl bromide (2.5 g) and the mixture was stirred at 70° C. for a day. Water was added to the reaction solution and extraction with ethyl acetate was conducted. The solvent was distilled off under reduced pressure and the resulting residue was subjected to purification by column chromatography using chloroform to give 4-cyclopentyl-7-methoxycarbonyl-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (2.5 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597820
Source datasetuspto-grants-1997_01
ORD IDord-66735cc8d2c34e6c9af0710ea4e9f539
Source noteuspto-grants-1997_01