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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481267Generated: October 31, 2026

indium(III)chloride → (S)-N-((S)-1-(4-Chloropyridin-2-yl)but-3-enyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1481267

Reaction equation

Participants

RoleNameHCIDCharge
Reactantindium(III)chlorideHCID 159675—
Reactant(NE,S)-N-[(4-chloro-2-pyridinyl)methylidene]-2-methylpropane-2-sulfinamideHCID 87132871—
ReactantHCID 178455850HCID 178455850—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(S)-N-((S)-1-(4-Chloropyridin-2-yl)but-3-enyl)-2-methylpropane-2-sulfinamideHCID 66744179115.1%

Reaction Steps

To a cooled (0-5° C.) mixture of indium(III) chloride (13.56 g, 61.3 mmol) in tetrahydrofuran (170 mL) was added dropwise over 30 min. allylmagnesium bromide (1M in diethylether) (62 mL, 61.3 mmol). The reaction was allowed to warm to rt. After 1 h at rt, a solution of 1A (10 g, 40.9 mmol) in ethanol (170 mL) was added. After 2-3 h, the reaction was concentrated under vacuum at 50-55° C. The crude material was partitioned between ethyl acetate (200 ml) and water (1×50 ml) and the layers were separated. The aqueous layer was extracted with ethyl acetate (2×50 ml). The organic layers were combined and washed with brine (1×100 ml), dried over sodium sulfate, filtered and concentrated to give 1B (13.5 g, 106%) as a yellow oil. MS (ESI) m/z: 287.2 (M+H)+. This material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409908B2
Source datasetuspto-grants-2016_08
ORD IDord-44df7cb44075484c85184a2a0b2d1e9a
Source noteuspto-grants-2016_08