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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503454Generated: October 30, 2026

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

https://huagongshe.com/reaction/1503454

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 M in 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 numberUS09212153B2
Source datasetuspto-grants-2015_12
ORD IDord-d87bef48d3b44f1dad9b2ae891eac739
Source noteuspto-grants-2015_12