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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506944Generated: October 30, 2026

Benzyl Bromide → HCID 10587639, compound

https://huagongshe.com/reaction/1506944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventDimethylformamideHCID 6228—
ProductHCID 10587639HCID 1058763980%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-butyl 3-hydroxyazetidine-1-carboxylate (21) (1 gm, 5.77 mmol) was dissolved in dry DMF (15 ml) and was cooled to 0° C. under nitrogen and was added sodium hydride (0.35 gm, 8.66 mmol). The reaction mixture was allowed to stir at room temperature for 30 min and was added benzylbromide (22; 1.08 gm, 6.35 mmol) at 0° C. The reaction mixture was then allowed warm to room temperature and stirred for 2 h. After completion of the reaction it was quenched by the addition of sat. ammonium chloride solution and extracted with ether. The organic layer was then dried over sodium sulfate and concentrated under vacuum. The crude product was purified column chromatography to yield compound 23 (1.21 gm, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221792B2
Source datasetuspto-grants-2015_12
ORD IDord-78daff80d57e463e89c893c1c4e27958
Source noteuspto-grants-2015_12