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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224836Generated: October 31, 2026

Lithium iodide → HCID 68871115, compound

https://huagongshe.com/reaction/2224836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 14494047HCID 14494047—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68871115HCID 6887111598%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-phenyl-propionic acid benzyl ester (2.0 g, 8.32 mmol), 4-bromo-2-methyl-2-butene (1.21 mL, 9.99 mmol), and lithium iodide (1 g) in tetrahydrofuran (15 mL) at 0° C. was treated dropwise with the lithium hexamethyldisilazide (9.99 mL, 1M in tetrahydrofuran, 9.99 mmol). The reaction was allowed to warm to 25° C. and stirred for 18 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the ethyl acetate layers were combined, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane, then 10% ethyl acetate in hexane, and 20% ethyl acetate in hexane to give the title compound (2.51 g, 98%). 1H NMR (300 MHz, CDCl3): δ ppm 1.53 (m, 6 H) 1.63 (m, 3 H) 2.60 (m, 1 H) 2.80 (m, 1 H) 4.94 (m, 1 H) 5.11 (m, 2 H) 7.26 (m, 10 H). MS (ESI+) m/z 326 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378414B2
Source datasetuspto-grants-2008_05
ORD IDord-8dd8a3b82a4348a49369b728edca9f90
Source noteuspto-grants-2008_05