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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087893Generated: November 2, 2026

2,3-Dihydroxybenzaldehyde → HCID 22164153, compound

https://huagongshe.com/reaction/1087893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DihydroxybenzaldehydeHCID 90579—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15058684HCID 15058684—
SolventEthanolHCID 702—
ProductHCID 22164153HCID 2216415389.4%

Reaction Steps

Under a dry nitrogen atmosphere a mixture of 6.0 grams (0.026 mole) of 2,3-di(2-fluoroethoxy)benzaldehyde (prepared by the method of Example 1 from 2,3-dihydroxybenzaldehyde) and 1.3 gram (0.034 mole) of sodium borohydride in 130 ml of ethanol was stirred at room temperature for approximately 18 hours. The reaction was quenched with dilute hydrochloric acid, and the mixture was extracted with diethyl ether. The extract was washed with dilute hydrochloric acid followed by an aqueous, saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 5.4 grams of 1,2-di-(2-fluoroethoxy)-3-hydroxymethylbenzene as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960884
Source datasetuspto-grants-1990_10
ORD IDord-0f77282acf3d44e48b67862c62af58d7
Source noteuspto-grants-1990_10