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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425186Generated: October 30, 2026

Benzyl Bromide → HCID 59382283, compound

https://huagongshe.com/reaction/425186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Bis-benzyloxy-5-isopropenyl-N-(4-morpholin-4-ylmethyl-phenyl)-benzamideHCID 66701698—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59382283HCID 5938228369.6%

Reaction Steps

2,4-Bis-benzyloxy-5-isopropenyl-N-(4-morpholin-4-ylmethyl-phenyl)-benzamide (0.245 g, 0.45 mmol) [prepared using Method A2 from (2,4-bis-benzyloxy-5-isopropenyl)-benzoic acid (Preparation B5) and 4-morpholin-4-yl-methyl-phenylamine] dissolved in DMF (3 ml), was treated with 60% NaH in mineral oil (27 mg, 1.5 eq) and stirred for 15 minutes followed by the addition of benzyl bromide (0.052 ml, 0.45 mmol), then stirred for a further 2 hours at room temperature. The reaction was diluted with EtOAc and water. The EtOAc layer was separated, washed with brine, dried (MgSO4) and evaporated to afford 0.2 g of the title compound as a yellow oil. MS: [M+H]+ 639.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106057B2
Source datasetuspto-grants-2012_01
ORD IDord-c03ae0f0500849d08af2c5fa83e00ab0
Source noteuspto-grants-2012_01