HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747159Generated: October 31, 2026
HCID 86688427, compound → HCID 86688426, compound
https://huagongshe.com/reaction/1747159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86688427 | HCID 86688427 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86688426 | HCID 86688426 | 52% |
Reaction Steps
To a stirred solution of the crude (S)—N-(4-chloro-2-(trifluoromethyl)benzylidene)-2-methylpropane-2-sulfinamide (26.8 g, 86.0 mmol) in dichloromethane (290 mL) at −48° C. was added a solution of methyl magnesium bromide (3.0 M in diethyl ether, 63.0 mL, 189.0 mmol) dropwise. The reaction was stirred below −40° C. for 18 h, and the reaction was slowly warmed to 0° C. and quenched with 50% saturated aqueous ammonium chloride solution (100 mL). The phases were separated, and the organic layer was washed with deionized water (50 mL). The aqueous layer was further extracted with ethyl acetate (2×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude material was purified by flash chromatography (SiO2, 50% ethyl acetate in hexanes) to afford the desired product (14.6 g, 44.5 mmol, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150550B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-769d3007b0874727b4e0ee4fe1d5f611 |
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| Source note | uspto-grants-2015_10 |
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