Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528765Generated: October 30, 2026

Benzyl Bromide → HCID 67979349, compound

https://huagongshe.com/reaction/528765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67979310HCID 67979310—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67979349HCID 67979349—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 200 mg (0.56 mmol) 10-(3-hydroxy-azetidin-1-yl)-5,6,8,9-tetrahydro-1,4,7,10a-tetraaza-cyclohepta[f]indene-7-carboxylic acid tert-butyl ester in 10 mL anhydrous THF maintained at 0° C. for 30 minutes was added 320 mg (6.72 mmol, 60% dispersion in mineral oil) NaH under an atmosphere of nitrogen and the reaction was stirred at 0° C. for 30 minutes. 0.8 mL (6.80 mmol) benzyl bromide was added and the reaction was heated at 65° C. for 16 hours. The reaction mixture was allowed to cool to room temperature and the solvent was evaporated. 25 mL EtOAc was added and the organic layer was washed with H2O (2×20 mL), and dried over Na2SO4. After filtration and evaporation the product was purified by column chromatography (silica, heptane/EtOAc 3:7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-3878d1fae6b54cc4ae5ee806c46a3a4e
Source noteuspto-grants-2016_05