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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981758Generated: November 3, 2026

Benzyl Alcohol → HCID 11075036, compound

https://huagongshe.com/reaction/981758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantD-Malic acidHCID 92824—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11075036HCID 1107503664%

Reaction Steps

To a solution of D-malic acid (18.8 g., 140.2 mmole) in 150 ml. of freshly-distilled THF was added dicyclohexylcarbodiimide (DCC, 1.1 equiv.) and the mixture was stirred at room temperature for 45 minutes. The reaction mixture was filtered to remove the precipitate of dicyclohexylurea which formed. The precipitate was washed with two 50 ml. portions of THF and the washings were combined with the filtrate. To the combined filtrate and washings were added two equivalents of benzyl alcohol and the solution was stirred overnight at room temperature. The reaction mixture was evaporated to remove the solvent and the residual oil containing the monoester was dissolved in 100 ml. of ethyl acetate. The solution was extracted with three 50 ml. portions of a 10% solution of sodium carbonate in water and the extracts were combined, acidified to pH 2 and extracted with three 50 ml. portions of ethyl acetate. The extracts were combined, washed with 25 ml. of brine, dried over magnesium sulfate, filtered, and then evaporated to dryness to yield D-malic acid monobenzyl ester as an oil in 64% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992544
Source datasetuspto-grants-1991_02
ORD IDord-d06dca65fe084fdd887a43e79a081a94
Source noteuspto-grants-1991_02