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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377361Generated: October 25, 2026

Hydrochloric Acid → HCID 15860332, compound

https://huagongshe.com/reaction/377361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-(Methylsulfonyl)benzaldehydeHCID 220376—
ReactantSodium MethoxideHCID 10942334—
Reactant5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethaneHCID 13933293—
SolventMethanolHCID 887—
ProductHCID 15860332HCID 15860332—

Reaction Steps

5-Fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane (15 g, 0.072 mol), p-methylsulfonylbenzaldehyde (14.0 g, 0.091 mol) and sodium methoxide (13.0 g, 0.24 mol) are heated in methanol (200 ml) at 60° C. under nitrogen with stirring for 6 hours. The reaction mixture is poured onto ice-water (750 g), and is acidified with 2.5N hydrochloric acid. The collected solid is triturated with a little ether to produce (Z)-5-fluoro-2-methyl-1-(p-methylsulfonylbenzylidene)-1H-3-indenyl-(2-hydroxy) ethane. Recrystallization of the crude reaction product results in the separation of the mixture of geometrical isomers (Z/E) and gives the title compound (R1 =5-fluror, R2 =CH3, R3 =H, R4 =CH2OH, n=1, R5 =CH3SO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025394
Source datasetuspto-grants-2000_02
ORD IDord-0c443b68506842a49d541f85a1283d38
Source noteuspto-grants-2000_02