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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584789Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 21220841, compound

https://huagongshe.com/reaction/1584789

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,3-PropanediolHCID 10442—
Reactant5-Bromo-1-benzofuran-7-carbaldehydeHCID 21220840—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 21220841HCID 21220841—

Reaction Steps

A mixture of 5-bromo-benzofuran-7-carbaldehyde (400 mg), 4-methylphenylsulphonic acid (0.38 g) and 1,3-propanediol (10 ml) in toluene (15 ml) was heated at reflux for 19 h, with azeotropic removal of water by Dean-Stark Apparatus. The reaction mixture was cooled, diluted with water (80 ml) and extracted with toluene (30 ml). The organic phase was dried, filtered and the filtrate evaporated in vacuo to give a brown oil. Purification by FCC eluted with hexane:ethyl acetate (7:1→3:1) gave the title compound as a yellow solid (427 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935972
Source datasetuspto-grants-1999_08
ORD IDord-dff727f3609941ad817f819b763562ab
Source noteuspto-grants-1999_08