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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585336Generated: October 30, 2026

Hydrochloric Acid → [2-Bromo-5-(hydroxymethyl)phenyl]methanol

https://huagongshe.com/reaction/585336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-Bis(acetoxymethyl)bromobenzeneHCID 9948291—
Reactant2,6-Bis(acetoxymethyl)bromobenzeneHCID 22340640—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product[2-Bromo-5-(hydroxymethyl)phenyl]methanolHCID 1296888483.9%

Reaction Conditions

Temperature10 °C

Reaction Steps

An about 93:7 mixture (36.7 g) of 2,4-bis(acetoxymethyl)-bromobenzene and 2,6-bis(acetoxymethyl)bromobenzene was dissolved in methanol (183 ml) and cooled to 10° C. To this solution was added dropwise 10% aqueous sodium hydroxide solution (133 g). The reaction mixture was stirred at room temperature for 1 hr, and the solvent (about 200 ml) was evanorated The residue was neutralized with dilute hydrochloric acid (about 200 ml). To the neutralized solution was added toluene (150 ml) and the mixture was stirred at 80-85° C. for 1 hr and cooled. The resulting crystals were collected by filtration and dried under reduced pressure to give an about 93:7 mixture (22.2 g, 83.7%) of 2,4-bis(hydroxymethyl)bromobenzene and 2,6-bis(hydroxymethyl)-bromobenzene as almost white crystals. 2,4-bis(Hydroxymethyl)-bromobenzene was isolated by preparative HPLC and used in the measurement.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930211B2
Source datasetuspto-grants-2005_08
ORD IDord-b2db50ced2fa4bb6aa9273dd5fc22918
Source noteuspto-grants-2005_08