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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509345Generated: October 30, 2026

Water → HCID 86675071, compound

https://huagongshe.com/reaction/1509345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58288757HCID 58288757—
SolventAcetonitrileHCID 6342—
ProductHCID 86675071HCID 8667507154.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

In 100 mL of acetonitrile, 25.5 g of a liquid of 2-hydroxy-1,1-difluoroethanesulfonyl chloride (purity: 98%, equivalent to 0.138 mol) was dissolved by stirring. The resulting solution was cooled to 0° C., admixed with 14.0 g (0.166 mol) of sodium hydrogencarbonate and 24.8 g (0.152 mol) of N-hydroxyphthalimide, and then, reacted at 0° C. for 24 hours. To the thus-obtained reaction solution, 125 mL of water was added. The reaction solution was subsequently extracted twice with 100 mL of ethyl acetate. The resulting organic layer was washed twice with 100 mL of water and subjected to concentration. The concentration residue was admixed with 75 mL of ethyl acetate, followed by heating the solution at 60° C. to dissolve the solid substance. Then, 150 mL of heptane was dropped into the solution. The solution was gradually cooled to 0° C. to precipitate a crystalline out of the solution. The crystalline precipitate was filtered out and dried. With this, 23.2 g of the target compound was obtained as a white solid (yield: 53%, purity: 97%, pure content: 22.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221928B2
Source datasetuspto-grants-2015_12
ORD IDord-be3e9c54c6dd4fbe9741eacf75481c1c
Source noteuspto-grants-2015_12