Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870992Generated: October 29, 2026

Hydrochloric Acid → HCID 18694168, compound

https://huagongshe.com/reaction/1870992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium FluorideHCID 522689—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantHCID 18694182HCID 18694182—
CatalystIron chloride (FeCl3)HCID 24380—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 18694168HCID 1869416816.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of (±)-methyl 6fluoro-3,4-dihydro-8-iodo-2H-1-benzopyran-2-carboxylate (0.026 mol), (trifluoromethyl)trimethylsilane (0.081 mol), cuprous iodide (0.1 mol) and kalium fluoride (0.081 mol) in a mixture of DMF (50 ml) and 1-methyl-2-pyrrolidinone (50 ml) was stirred for 3 h at 60° C. The cooled reaction mixture was poured out into a solution of iron (III) chloride (200 g) and hydrochloric acid (50 ml) in water (300 ml). This mixture was extracted three times with diethyl ether (150 ml). The combined organic layers were washed with a 5% aqueous Na2S2O3 solution (decolorization), dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent: CH2Cl2). The pure fractions were collected and the solvent was evaporated, yielding 5.7 g (78.8%). This fraction was recrystallized from DIPE. The precipitate was filtered off and dried, yielding 1.2 g(16.6%) (±)-methyl 6-fluoro-3,4-dihydro-8-(trifluoromethyl)-2H-1-benzopyran-2-carboxylate; mp. 71.8° C. (interm 4-b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100268
Source datasetuspto-grants-2000_08
ORD IDord-1aba8e4a8a1d4557903f24d4eed91551
Source noteuspto-grants-2000_08