HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175590Generated: October 31, 2026
HCID 58562506, compound → HCID 58562811, compound
https://huagongshe.com/reaction/2175590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58562506 | HCID 58562506 | — |
| Reactant | HCID 178461633 | HCID 178461633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58562811 | HCID 58562811 | — |
Reaction Steps
A solution of (E)-N-(1,4-dioxaspiro[4.5]decan-8-ylmethylene)-2-methylpropane-2-sulfinamide (as prepared in of Example 11 Step A, 3.66 g, 13.4 mmol) in dry THF (100 mL) was placed under an argon atmosphere and treated with ethylmagnesium chloride dropwise. After stirring at ambient temperature for 2 hours, the reaction mixture was cooled to −10° C. and cautiously quenched by the addition of saturated ammonium chloride solution. After dilution with water and ether extraction, the organic layer was concentrated in vacuo. Purification of the residue by flash chrom (silica gel, ethyl acetate) afforded the titled compound as a solid. 1H NMR (CHLOROFORM-d) δ: 3.80-4.00 (m, 4H), 2.85-3.15 (series of m, 2H), 1.71 (series of m, 11H), 1.20-1.25 (s, 9H), 0.97 (t, J=7.5 Hz, 3H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062048B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-e2f697c37ba24269a6ee9394f282abc0 |
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| Source note | uspto-grants-2015_06 |
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