HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365495Generated: October 31, 2026
HCID 87263096, compound → HCID 67086720, compound
https://huagongshe.com/reaction/2365495
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 87263096 | HCID 87263096 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67086720 | HCID 67086720 | — |
Reaction Steps
To a solution of 2-Methyl-propane-2-sulfinic acid [4-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-phenyl]-but-(E)-ylidene]-amide (4.51 g, 11.8 mmol) in THF (120 ml) at 0° C. is added vinylmagnesium bromide (11.8 ml of a 1 M solution in THF, 11.8 mmol) dropwise. After addition is complete, the mixture is stirred at 0° C. for 30 minutes then quenched with sat. aq. NH4Cl solution (20 ml). This mixture is allowed to warm to room temperature and diluted with water (50 ml) and EtOAc (50 ml). The organic phase is separated, dried (MgSO4) and concentrated in vacuo. Purification by chromatography (SiO2, EtOAc/iso-hexane) affords 2-Methyl-propane-2-sulfinic acid {4-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-phenyl]-1-vinyl-butyl}-amide as a mixture of diastereomers as a gum; [M+H]+ 410.39
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697687B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8a8713a698b3472fbea61591e4055eb3 |
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| Source note | uspto-grants-2014_04 |
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