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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2573Generated: October 26, 2026

Bromoform → [2-Chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-hydroxy acetic acid

https://huagongshe.com/reaction/2573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-DioxaneHCID 31275—
ReactantLithium ChlorideHCID 433294—
Reactant2-Chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy]benzaldehydeHCID 18359091—
SolventWaterHCID 962—
Product[2-Chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-hydroxy acetic acidHCID 18359099—

Reaction Conditions

Temperature0 °C

Reaction Steps

2.42 g of lithium chloride and 7.02 g of potassium hydroxide were dissolved in 30 ml of water at 0° C. and a solution of 10 g of 2-chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy] benzaldehyde (synthesized in Preparation 1), 2.8 ml of bromoform and 38 ml of dioxane were added to this mixture. The mixture was stirred for 24 hours at 0° C. and then another 2.8 ml of bromoform were added. The mixture stood for 16 hours and after dilution with 100 ml of water, the solution was washed with ether, decanted, cooled to 0° C. and acidified until the pH was 2.5-3. Extraction was carried out with ether and the organic phase was washed with water and dried. The solvent was driven off to collect 11.4 g of the desired product in the form of an oil with a Rf=0.1 [eluant: methylene chloride--methanol--acetic acid (89-10-1)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728828
Source datasetuspto-grants-1998_03
ORD IDord-30ada60bc0e74527b46c8f5abdf6a8c0
Source noteuspto-grants-1998_03