HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931555Generated: October 25, 2026
tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-(tert-butylsulfinylimino)acetate
https://huagongshe.com/reaction/931555
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Reactant | Ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-oxoacetate | HCID 57475646 | — |
| Reactant | HCID 178445888 | HCID 178445888 | — |
| Product | (S)-ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-(tert-butylsulfinylimino)acetate | HCID 86658358 | 51% |
Reaction Steps
A flask was charged with (S)-2-methylpropane-2-sulfinamide (0.764 g, 6.31 mmol) and neopentylzinc(II) iodide (0.5 M in THF, 10.0 mL, 5.00 mmol) was added under nitrogen atmosphere. The mixture was stirred at RT for 15 minutes and ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-oxoacetate (1.00 g, 3.15 mmol) was added in one portion. The reaction mixture was quenched with saturated aqueous ammonium chloride after 8 h. The reaction was partitioned between EtOAc and water. The organic phase was separated, washed with NH4Cl, water and brine. The organic phase was dried over MgSO4 and the solvent was removed under reduced pressure. The crude material was purified by silica gel chromatography (10-30% EtOAc/hexane) to provide 0.675 g (S)-ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-(tert-butylsulfinylimino)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296759B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-c0374a2d06684bd39f54daca3f787e62 |
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| Source note | uspto-grants-2016_03 |
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