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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162943Generated: October 29, 2026

Benzyl Bromide → Tetrabenzylpentaerythritol

https://huagongshe.com/reaction/1162943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPentaerythritolHCID 8285—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
SolventDimethylformamideHCID 6228—
ProductTetrabenzylpentaerythritolHCID 1208252838%

Reaction Steps

Sodium hydride (440 mg, 11.01 mmol) and benzyl bromide (1.3 mL, 11.01 mmol) were added to 20 mL of a solution of pentaerythritol (500 mg, 3.67 mmol) in DMF, and the mixture was stirred at room temperature for 14 hours. Aqueous saturated ammonium chloride was added to the mixture, followed by extraction with ethyl acetate. The extract was washed with saturated saline and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to obtain 3-benzyloxy-2,2-bis(benzyloxymethyl)propan-1-ol (560 mg, 38%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820693B2
Source datasetuspto-grants-2010_10
ORD IDord-3fbdb400f3c4428d914202e1fbe3853f
Source noteuspto-grants-2010_10