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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223602Generated: October 23, 2026

(+-)-4-Hydroxymandelic acid → p-Nitrobenzyl 4-hydroxymandelate

https://huagongshe.com/en/reaction/223602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-4-Hydroxymandelic acidHCID 328—
ReactantDimethylacetamideHCID 31374—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
Productp-Nitrobenzyl 4-hydroxymandelateHCID 1306646084%

Reaction Steps

To a solution of 16.8 g. (0.1 mole) of 4-hydroxymandelic acid in 300 ml. of dimethylacetamide were added 11.2 g. of potassium t-butoxide with an additional 100 ml. of dimethylacetamide. The mixture was stirred at room temperature until a solution was obtained. p-Nitrobenzyl bromide (21.6 g., 0.1 mole) was added to the solution followed by 100 ml. of additional dimethylacetamide. The reaction mixture was stirred for 24 hours and was diluted with one liter of ethyl acetate. The mixture was washed repeatedly with water and dried over magnesium sulfate. The dried solution was evaporated to yield 25 g. (84 percent yield) of p-nitrobenzyl 4-hydroxymandelate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355172
Source datasetuspto-grants-1982_10
ORD IDord-97b1b52820544c818657c0ef02c23237
Source noteuspto-grants-1982_10