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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292760Generated: October 30, 2026

Benzyl Bromide → HCID 21191857, compound

https://huagongshe.com/reaction/2292760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10589888HCID 10589888—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 21191857HCID 2119185782%

Reaction Steps

5-Hydroxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamide (400 mg, 1.4 mmol) was dissolved in 50 mL of DMSO, 40 mg (1.0 mmol) of 60% NaH/mineral oil added, stirred approximately 0.5 hour, 0.2 mL of benzyl bromide added and stirring maintained 2.5 hours. The mixture was diluted with water, extracted with EtOAc, the EtOAc solution washed with water, saturated NaCl solution, dried (Na2SO4), and concentrated at reduced pressure. The residue was chromatographed on silica (eluted with a gradient, CH2Cl2 →2% MeOH/CH2Cl2) and crystallized from CH2Cl2 /MeOH to give 440 mg (82% yield) of 5-benzyloxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamide, mp, 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684034
Source datasetuspto-grants-1997_11
ORD IDord-6c6b4c8c6aaf425d8a6322d52aa2c4f3
Source noteuspto-grants-1997_11