HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596003Generated: October 30, 2026
tert-Butylsulfinamide, (S)-(-)- → HCID 118045320, compound
https://huagongshe.com/reaction/596003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Reactant | 3-Bromo-5-fluorobenzaldehyde | HCID 21986246 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 118045320 | HCID 118045320 | 99.4% |
Reaction Steps
To a solution of 3-bromo-5-fluorobenzaldehyde (5 g, 24.63 mmol) and (S)-2-methylpropane-2-sulfinamide (3.28 g, 27.1 mmol) in DCE (82 mL) was added copper(II) sulfate (anhydrous) (7.86 g, 49.3 mmol). The suspension was stirred under nitrogen at 60° C. overnight. The reaction mixture was cooled down, filtered through a plug of celite, and rinsed with DCM. The filtrate was concentrated to yield the crude product. The crude product was purified by flash chromatograph eluting with 0-30% EtOAc in heptane to yield the product (S,E)-N-(3-bromo-5-fluorobenzylidene)-2-methylpropane-2-sulfinamide (7.5 g, 24.49 mmol, 99% yield) as a light yellow color oil. LCMS (m/z): 306.1/308.1 (MH+), 1.04 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-51693e601ff34f6eb4acbfbcc2155695 |
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| Source note | uspto-grants-2016_01 |
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