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
Participants
| Role | Name | HCID | Charge |
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| Reactant | indium(III)chloride | HCID 159675 | — |
| Reactant | (NE,S)-N-[(4-chloro-2-pyridinyl)methylidene]-2-methylpropane-2-sulfinamide | HCID 87132871 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-N-((S)-1-(4-Chloropyridin-2-yl)but-3-enyl)-2-methylpropane-2-sulfinamide | HCID 66744179 | 115.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409908B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-44df7cb44075484c85184a2a0b2d1e9a |
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| Source note | uspto-grants-2016_08 |
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