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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854115Generated: October 30, 2026

HCID 14467914, compound → HCID 58659580, compound

https://huagongshe.com/reaction/854115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14467914HCID 14467914—
ReactantHCID 178506852HCID 178506852—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58659580HCID 58659580—

Reaction Steps

Preparation of (S)-picolinyl t-butylsulfoxide from (S)-tert-Butyl (1R, 2S)-aminoindanol 4-toluene sulfonamide sulfinate: To a picolinyl lithium solution (2 mL, 0.6 M) in THF at −78° C. was added (S)-t-butyl-(1R, 2S)-aminoindanol tosylate sulfinate (130 mg, 0.30 mmol). The mixture was warmed to room temperature and stirred until the starting material was consumed as monitored by TLC. The reaction was quenched by aq. NaHCO3 (20 mL) and diluted with ethyl acetate (20 mL), and the organic phase was washed with water (20 mL) and brine (20 mL). The organic layer was concentrated in vacuo and the residue was purified by chromatography eluted with ethyl acetate to yield 32 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256297B2
Source datasetuspto-grants-2007_08
ORD IDord-5ccc389c81d04c8caf6bfead3b78ebf8
Source noteuspto-grants-2007_08