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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048512Generated: November 1, 2026

Allyl bromide → HCID 58573449, compound

https://huagongshe.com/reaction/1048512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 58573348HCID 58573348—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58573449HCID 58573449—

Reaction Steps

A solution of lithium bis(trimethylsilyl)amide (1M in THF, 0.165 mL, 0.165 mmol) was added dropwise at −78° C. to a solution of (S)-tert-butyl 2-(2S,3R)-3-(3-chlorophenyl)-2-(4-chlorophenyl)-6-oxopiperidin-1-yl)-2-cyclopropylacetate (Example 249, Step C, 71 mg, 0.15 mmol) and allyl bromide (15.54 uL, 0.165 mmol) in 0.5 mL of THF. The reaction was allowed to warm to ambient temperature. After stirring for 2 h, the reaction was quenched with sat. aqueous ammonium chloride solution and extracted with ethyl acetate. The combined organic layers were washed with sat. aq. NaCl solution and dried over sodium sulfate, then filtered and the filtrate was concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with ethyl acetate/hexane provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-adc7d01303de47619ddf768915cb31f5
Source noteuspto-grants-2013_10