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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799036Generated: November 1, 2026

Hydrochloric Acid → HCID 59492824, compound

https://huagongshe.com/reaction/1799036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDimethylformamideHCID 6228—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 59492525HCID 59492525—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59492824HCID 59492824—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of an optically active form (33.3 g) of t-butyl[4-(2-fluoro-9-hydroxy-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-acetate and paraformaldehyde (18.3 g) in dimethylformamide (100 ml) was added at room temperature a 1M solution (244 ml) of tetrabutylammonium fluoride in tetrahydrofuran, and the mixture was stirred at 90° C. for 4 hr. To the reaction mixture was added 1N hydrochloric acid (400 ml), and the mixture was extracted with ethyl acetate (200 ml). The separated aqueous layer was extracted twice with ethyl acetate (100 ml). The combined organic layer was successively washed once with 1N hydrochloric acid (100 ml), twice with brine (water/saturated brine=100 m1/10 ml) and once with saturated brine (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was azeotroped twice with toluene to give the title compound (28.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343994B2
Source datasetuspto-grants-2013_01
ORD IDord-081ad954969144b0986be59466c1e8f7
Source noteuspto-grants-2013_01