HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365496Generated: November 1, 2026
Tert-Butanesulfinamide → HCID 87263023, compound
https://huagongshe.com/reaction/2365496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | HCID 86641906 | HCID 86641906 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 87263023 | HCID 87263023 | — |
Reaction Steps
To a solution of 2-methyl-propane-2-sulfinic acid {4-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-phenyl]-1-formyl-butyl}-amide in THF (20 ml) is added tert-butyl sulfinamide (323 mg, 2.7 mmol) followed by titanium ethoxide (1.0 ml, 4.8 mmol). The yellow solution formed is stirred at room temperature overnight. The solution is quenched with 1N NaOH (50 ml) and EtOAc (50 ml) and stirred for 30 minutes at room temperature. The resultant mixture is filtered through Celite™ (filter material) and the organic phase separated and dried (MgSO4). Concentration gives 2-Methyl-propane-2-sulfinic acid (4-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-phenyl]-1-{[(E)-2-methyl-propane-2-sulfinylimino]-methyl}-butyl)-amide as a mixture of diastereomers as a yellow oil; [M+H]+ 515.38
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-89680ea08d8a42109774acddde5a4754 |
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| Source note | uspto-grants-2014_04 |
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