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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403338Generated: October 26, 2026

Sulfuric Acid → HCID 86681332, compound

https://huagongshe.com/reaction/403338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium MethoxideHCID 10942334—
Reactant(S)-1,2-Difluoro-3-(1-nitrohex-5-en-2-yl)benzeneHCID 86681331—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 86681332HCID 86681332138.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 250 mL round-bottomed flask was dissolved (S)-1,2-difluoro-3-(1-nitrohex-5-en-2-yl)-benzene (4.14 g, 17.2 mmol) in methanol (21 mL) under nitrogen. After cooling to 0° C., sodium methoxide (4.12 mL, 18.0 mmol) was added via syringe. After stirring at 0° C. for 30 min, the temperature was lowered to −60° C. Conc. sulfuric acid (2.93 mL, 54.9 mmol) in 21 mL methanol was added dropwise. The resulting milky mixture was stirred at −60 to −20° C. for 4 h. It was diluted with ethyl acetate and saturated ammonium chloride solution. The layers were separated. The aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine, dried, and concentrated to a give tan oil (4.8 g), which was dissolved in chloroform (124 mL) Water (31 mL) was added followed by slow addition of trifluoroacetic acid (31 mL). The mixture was stirred at rt overnight for 18 h. The layers were separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were dried and concentrated to give a light yellow oil (5 g, 100%). This was directly carried onto next reaction immediately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748429B2
Source datasetuspto-grants-2014_06
ORD IDord-de24a9419e4e461994706e497a961822
Source noteuspto-grants-2014_06