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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220565Generated: November 3, 2026

Hydrochloric Acid → HCID 70849514, compound

https://huagongshe.com/reaction/2220565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58991866HCID 58991866—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventPentaneHCID 8003—
ProductHCID 70849514HCID 70849514—

Reaction Conditions

Temperature90 °C

Reaction Steps

50.0 g (1.25 mol) of sodium hydride (60% suspension in mineral oil) are washed repeatedly with n-pentane and suspended in 3000 ml of toluene. The suspension is heated to 90° C., and a solution of 145.0 g (0.46 mol) of 8-(4-ethoxy-2,3-difluorophenyl)-1,4-dioxaspiro[4.5]decan-7-ol in 700 ml of DMF is slowly metered in. The batch is stirred at 90° C. for 30 h, cooled and hydrolysed using water. The mixture is neutralised by addition of 2 N hydrochloric acid, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed with sat. sodium chloride solution. The solution is dried using sodium sulfate and concentrated to dryness under reduced pressure. The crude product obtained is recrystallised from ethanol at 5° C., giving (±)-(4aR*, 9bS*)-7-ethoxy-6-fluoro-1,4,4a,9b-tetrahydro-2H-spiro-[dibenzo[b,d]-furan-3,2′-1,3-dioxolane] as colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417157B2
Source datasetuspto-grants-2008_08
ORD IDord-110bbf33604e44d1b11aed490f0749f1
Source noteuspto-grants-2008_08