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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985942Generated: November 3, 2026

N-bromobutanimide → HCID 68428555, compound

https://huagongshe.com/reaction/1985942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 68427426HCID 68427426—
ReactantHCID 178418443HCID 178418443—
SolventDimethyl SulfideHCID 1068—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68428555HCID 6842855559.5%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A slurry of copper bromide (I)-dimethyl sulfide complex (1.57 g, 7.66 mmol) in THF (20 mL) and dimethyl sulfide (10 mL) as co-solvent was cooled to −40° C. and ethyl magnesium bromide (5 mL, 15.3 mmol) was added dropwise for 10 min. The slurry was stirred for 40 min while warming to −15° C. The greenish slurry was cooled to −40° C. and (4R)-4-benzyl-3-[(2E)-5,5,5-trifluoropent-2-enoyl]1,3-oxazolidin-2-one (2 g, 6.38 mmol) was added dropwise as a solution in THF (5 mL) at −40° C. The reaction was allowed to warm to 25° C. overnight (20 h). The black slurry was cooled down to −78° C. and N-bromosuccinimide (2.3 g 12.76 mmol) was added portionwise. It was allowed to warm to −40° C. and stirred for an additional 30 min. After this period, the black slurry became greenish to blue. A precipitate formed and was filtered off. The mother liquor was diluted with EtOAc (150 mL) and the organic layer washed with saturated NaCl (50 mL). The organic layer was dried over MgSO4, filtered and concentrated to afford (4R)-4-benzyl-3-[(2R,3S)-2-bromo-3-ethyl-5,5,5-trifluoropentanoyl]-1,3-oxazolidin-2-one as a green semi-solid (1.6 g, 59.5%). Mass Spectrum (−ESI): 421, 420 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547725B2
Source datasetuspto-grants-2009_06
ORD IDord-c5b768dcbde0450c98d49badaf5ce697
Source noteuspto-grants-2009_06