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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828087Generated: October 30, 2026

Bromoform → HCID 69642653, compound

https://huagongshe.com/reaction/1828087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantPotassium HydroxideHCID 14797—
Reactant1-benzyl-1H-pyrazole-3-carbaldehydeHCID 11401199—
ReactantDioxane MethanolHCID 21966525—
SolventMethanolHCID 887—
ProductHCID 69642653HCID 69642653—

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl-1H-pyrazole-3-carbaldehyde (1.55 g, CAS 321405-31-6) and bromoform (0.94 ml) were dissolved under an argon atmosphere in dioxane/MeOH 1:1 (40 ml) and cooled to 0° C. A solution of KOH (2.31 g) in MeOH (20 ml) were added over a period of 20 min. The reaction was warmed to r.t. and stirred overnight. The reaction mixture was concentrated to one third of the volume, then taken up in water and washed with EtOAc. The aqueous layer was brought ot pH 1 with HCl, then extracted with EtOAc. The organic layer was washed with brine and concentrated to give crude (RS)-(1-benzyl-1H-pyrazol-3-yl)-methoxy-acetic acid (1.41 g). Yellow oil. MS 245.1 ([M−H]−)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056932B2
Source datasetuspto-grants-2006_06
ORD IDord-7c22297b020848f5b2e490550f5b8d6c
Source noteuspto-grants-2006_06