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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306126Generated: November 3, 2026

Glycerol → 3-(Benzyloxy)-1,2-propanediol

https://huagongshe.com/reaction/2306126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycerolHCID 753—
ReactantMethanolHCID 887—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product3-(Benzyloxy)-1,2-propanediolHCID 98072—

Reaction Steps

As an alternative procedure to a stirred solution of the protected glycerol (6.7 g, 0.05 mole) in dry THF (100 mL) was added NaH (1.8 g, 0.075 mole) portionwise at 0° C. The reaction mixture was refluxed for 1.5 h, and benzyl bromide (10.3 g, 0.06 mole) was added. The mixture was stirred at room temperature. Once the reaction was completed, 2 mL of methanol was added at 0° C. to destroy the excess of NaH. The reaction mixture was extracted with 3×50 mL of ethyl ether, and the combined ether layers dried over sodium sulfate. After solvent removal, the residue of (11.9 g, Y=61%). was combined with 60 mL of 10% acetic acid, then heated (oil bath, 100° C.), until the original emulsion disappeared (about 0.5 h), After concentration, the residue was distilled in vacuo, giving 8.1 g (b.p.116-118° C./50μ) (Y=89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441214B1
Source datasetuspto-grants-2002_08
ORD IDord-4a0ce279e2134307aa47bc45be97e65d
Source noteuspto-grants-2002_08