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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346398Generated: October 30, 2026

Catechol → HCID 15042466, compound

https://huagongshe.com/reaction/346398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantHydrochloric AcidHCID 313—
ReactantGlyoxylic AcidHCID 760—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium HydroxideHCID 14798—
ReactantCarbonate IonHCID 19660—
ReactantIodide IonHCID 30165—
ProductHCID 15042466HCID 15042466—

Reaction Conditions

Temperature40 °C

Reaction Steps

500 ml of an aqueous solution containing 48 g (1.2 mol) of sodium hydroxide was dropwise added to a suspension of 88 g (0.8 mol) of catechol and 109.5 g (about 0.5 mol) of a 40% glyoxylic acid aqueous solution under a nitrogen atmosphere under cooling with ice, and heated to 40° C. for 5 hours. The reaction solution was adjusted to pH2.0 with 6N hydrochloric acid under cooling with ice, and unreacted catechol was extracted with ethyl acetate. The water layer was evaporated to dryness under reduced pressure. The residue was dissolved in 700 ml of N,N-dimethylformamide and 276 g (2 mol) of pottasium carbonate, 10 g (60 mmol) of pottasium iodide and 230 ml (2 mol) of benzylchloride were added thereto. The mixture was stirred for 15 hours at room temperature and further stirred for 8 hours at 40° C. The reaction solution was poured into 1.5 liter of ice water and extracted with ethyl acetate, followed by washing with water and a saturated sodium chloride aqueous solution. The extract was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain crude benzyl 3,4-dibenzyloxymandelate. 1 liter of methanol and 200 ml of an aqueous solution containing 60 g of sodium hydroxide were added to the residue and stirred for 5 hours at room temperature. The reaction solution was concentrated under reduced pressure, and 1 liter of ice water was added to the residue. The solution was adjusted to pH2.0 with concentrated hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and concentrated under reduced pressure. After cooling, the precipitated crystals were collected and washed with isopropyl ether to obtain 83 g (yield: 45.5%) of 3,4-dibenzyloxymandelic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061794
Source datasetuspto-grants-1991_10
ORD IDord-0b9b071cc7734dff952e64c0b7e96632
Source noteuspto-grants-1991_10