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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473030Generated: October 26, 2026

Lithium Hexamethyldisilazide → Tert-butyl 3-(4-bromo-2-iodobenzyl)-3-cyanoazetidine-1-carboxylate

https://huagongshe.com/reaction/473030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-Boc-3-cyanoazetidineHCID 10631283—
Reactant4-Bromo-1-(bromomethyl)-2-iodobenzeneHCID 53231307—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-(4-bromo-2-iodobenzyl)-3-cyanoazetidine-1-carboxylateHCID 5819757375.3%

Reaction Steps

To a solution of tert-butyl 3-cyanoazetidine-1-carboxylate (2.1774 g, 11.95 mmol) and 4-bromo-1-(bromomethyl)-2-iodobenzene (5.0227 g, 13.36 mmol) in THF (30 mL) was added LiHMDS (1.0 Min THF, 15 mL, 15 mmol) at −78° C. The mixture was allowed to slowly warm to room temperature over 20 h. The reaction mixture was then quenched with saturated NH4Cl, extracted with EtOAc, and dried over Na2SO4. After the solvent was evaporated under reduced pressure, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 4.2959 g (75%) of tert-butyl 3-(4-bromo-2-iodobenzyl)-3-cyanoazetidine-1-carboxylate as foam. LC-MS tR=2.17 min in 3 min chromatography, m/z 477, 479 (MH+), 462, 464 (MH+-15), 421, 423 (MH+-56).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633212B2
Source datasetuspto-grants-2014_01
ORD IDord-1e093c0edfa24f6cb7b0ed6713f9c84f
Source noteuspto-grants-2014_01