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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307397Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 12132429, compound

https://huagongshe.com/reaction/2307397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12132428HCID 12132428—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12132429HCID 12132429—

Reaction Steps

A stirred solution of t-butyl (2S)-2-[(1H-indol-4-yloxy)methyl]-1-pyrrolidinecarboxylate (1.23 g, 3.89 mmol) in THF is treated with sodium hydride (0.17 g, 60% in mineral oil, 4.28 mmol) under nitrogen at room temperature, stirred for 30 minutes, treated with benzenesulfonyl chloride (0.55 mL, 4.28 mmol), stirred at room temperature for 22 h, quenched with ice-water and diluted with EtOAc. The organic phase is separated, washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (siliga gel, EtOAc/hexanes, 2/8) to afford the title compound as an off-white foam, 1.21 g, mp 48-50° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831094B2
Source datasetuspto-grants-2004_12
ORD IDord-466ab3a9853e4bc68445865c59c4ff88
Source noteuspto-grants-2004_12