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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934610Generated: October 27, 2026

Bromoform → Methyl 2-(benzo[d][1,3]dioxol-5-yl)-2-hydroxyacetate

https://huagongshe.com/reaction/1934610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantPiperonalHCID 8438—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-DioxaneHCID 31275—
ReactantLithium ChlorideHCID 433294—
CatalystSulfuric AcidHCID 1118—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-hydroxyacetateHCID 273389—

Reaction Steps

Lithium chloride (11.8 g), potassium hydroxide (31.4 g) and tetrabutylammonium bromide (4.5 g) were dissolved in a mixture of 1,4-dioxane (120 ml) and water (120 ml). Piperonal (21 g, 140 mmol) was added to this vigorously stirred ice-cold mixture, and after 10 minutes bromoform (12.2 ml 140 mmol) was added dropwise over ˜30 minutes. Stirring was continued for 20 hours at ambient temperature. Water (500 ml) was added and the mixture warmed to dissolve the precipitate. After washing with diethylether, the aqueous solution was acidified with concentrated hydrochloric acid. The crude carboxylic acid intermediate was isolated by extraction with diethylether and evaporation in vacuo. The residue was dissolved in methanol (500 ml) and acidified with 20 drops of concentrated sulphuric acid. The solution was heated to reflux for 2 hours, then cooled and evaporated in vacuo. The residue was dissolved in diethylether and washed with water. The organic fraction was dried (magnesium sulphate), and concentrated in vacuo. Flash chromatography using dichloromethane as eluant, and then recrystallisation from diisopropylether gave 13.2 g of the subtitle compound. (m.p. 93-95° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384070B2
Source datasetuspto-grants-2002_05
ORD IDord-fd2027222e444febb609469decbf44eb
Source noteuspto-grants-2002_05