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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477598Generated: October 25, 2026

Water → 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone

https://huagongshe.com/reaction/477598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 13957955—
SolventDimethylformamideHCID 6228—
Product3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 1401424425%

Reaction Conditions

Temperature0 °C

Reaction Steps

50% Oily sodium hydride (0.21 g) was suspended in N,N-dimethylformamide (5 ml), and the resultant suspension was cooled to 0° C. 6-Fluoro-5-nitro-2(3H)-benzothiazolone (1.0 g) was portionwise added thereto at 0° C., and the mixture was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (0.86 g) was added to the reaction mixture at 0° C., and the temperature was gradually elevated to a temperature of 50° to 60° C., followed by stirring at that temperature for 3 hours. Water was added to the mixture, which was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9) to give 0.35 g of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone, m.p., 139.0°-140.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888428
Source datasetuspto-grants-1989_12
ORD IDord-33779e788a05417badbe4024f628ef3d
Source noteuspto-grants-1989_12