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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250031Generated: November 2, 2026

Hydrochloric Acid → 5-Chloro-1-(4-fluorophenyl)-1H-indole

https://huagongshe.com/reaction/1250031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Chloro-1-(4-fluorophenyl)-1H-indol-3-yl acetateHCID 10924714—
SolventEthanolHCID 702—
Product5-Chloro-1-(4-fluorophenyl)-1H-indoleHCID 10236188—

Reaction Steps

1-(4-flourophenyl)-3-acetoxy-5-chloroindole (100.0 g, 0.33 mol) was dissolved in 1000 mL EtOH. During the next hour sodium borohydride pellets (18.7 g, 1.5 eq.) were added batchwise at reflux. The reaction mixture was stirred over night at reflux and cooled to room temperature. Concentrated HCl (appr. 50 mL until pH 1) was added and the reaction mixture was stirred at room temperature for 1 hour. 200 mL demineralized water was added, and the resulting suspension was filtrated. The filter cake was washed with further 50 mL water and 10 mL EtOH. The product was dried over night in vacuum at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335463B1
Source datasetuspto-grants-2002_01
ORD IDord-e395ac259c25496d9df308b94b7242bd
Source noteuspto-grants-2002_01