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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589881Generated: November 4, 2026

Sodium Thiosulfate → HCID 66584943, compound

https://huagongshe.com/reaction/589881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 66584760HCID 66584760—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66584943HCID 6658494333.4%

Reaction Steps

To a solution of 38.3 g (164 mmol) of ethyl 4-(3-fluorophenyl)-1H-pyrrole-3-carboxylate in 380 ml of tetrahydrofuran are added, over 30 minutes, 32.1 g (181 mmol) of N-bromosuccinimide (CAS 128-08-5), and the mixture is then stirred for 3 hours at reflux. After cooling, 200 ml of aqueous 5% sodium thiosulfate solution are added and the reaction product is extracted with ethyl acetate. The organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure, to give 17.1 g of ethyl 5-bromo-4-(3-fluorophenyl)-1H-pyrrole-3-carboxylate in the form of a white powder after recrystallizing from diisopropyl ether, filtering off and drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233965B2
Source datasetuspto-grants-2016_01
ORD IDord-b0903ec3b8244e43a709dea1b835d2eb
Source noteuspto-grants-2016_01