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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840196Generated: October 31, 2026

2-Fluoroethyl bromide → 1-(2-Fluoroethyl)-5-nitro-1,3-dihydro-2h-2,1-benzisothiazole-2,2-dione

https://huagongshe.com/reaction/840196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoroethyl bromideHCID 12982—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Nitro-1,3-dihydrobenzo[c]isothiazole 2,2-dioxideHCID 15538710—
SolventWaterHCID 962—
Product1-(2-Fluoroethyl)-5-nitro-1,3-dihydro-2h-2,1-benzisothiazole-2,2-dioneHCID 2262276267%

Reaction Conditions

Temperature80 °C

Reaction Steps

NaHCO3 (0.93 g, 11.0 mmol) is dissolved in H2O (15 mL) and 5-Nitro-1,3-dihydro-2H-2,1-benzisothiazole-2,2-dione (1) (1.90 g, 8.9 mmol) is added with stirring. The mixture is heated to 80° C. for 0.5 hrs and a yellow solid formed. The mixture is cooled to 0° C. and filtered. The solid is washed with cold H2O (15 mL) then with cold EtOH (25 mL). The yellow solid thus obtained is dried under high vacuum then dissolved in dry DMF (15 mL). 1-Bromo-2-fluoroethane (1.52 mL, 20.0 mmol) is added and the solution heated to 100° C. for 4 hrs. The solution is cooled to room temperature then poured into ice water (50 mL). The solid is collected by filtration and gave crystals (1.55 g, 67%) after recrystallization from EtOH. Mp 142-4° C. HRMS (FAB) calcd for C9H9FN2O4S +NA1 283.0165, found 283.0166.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365612B2
Source datasetuspto-grants-2002_04
ORD IDord-694c4096000c4d0cbab2205b160e4118
Source noteuspto-grants-2002_04