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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917414Generated: November 1, 2026

Allyl bromide → HCID 67490756, compound

https://huagongshe.com/reaction/1917414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 67490827HCID 67490827—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67490756HCID 6749075687.5%

Reaction Conditions

Temperature-5 °C

Reaction Steps

(4S)-4-(tert-Butyldimethylsilyloxy)methyl-2-oxo-1-[(1R)-1-phenylethyl]pyrrolidine (333.5 g, 1.00 mol) and allyl bromide (90.9 mL, 1.05 mol) were dissolved in tetrahydrofuran (1.10 L). Lithium hexamethyldisilazide (1.0 M solution in tetrahydrofuran) (1.10 L, 1.10 mol) was added dropwise at −15° C., and the mixture was stirred at −5° C. for one hour. The reaction solution was extracted with a saturated ammonium chloride solution and ethyl acetate. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Thereafter, the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:ethyl acetate=4:1→2:1) to give 327 g of the title compound as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618094B2
Source datasetuspto-grants-2013_12
ORD IDord-720548660d6944559c5022131f27c71d
Source noteuspto-grants-2013_12