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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106872Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 86743282, compound

https://huagongshe.com/reaction/2106872

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 86743283HCID 86743283—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 86743282HCID 8674328276%

Reaction Steps

A solution of t-butyl 2-bromo-7-phenyl-(2E)-hepten-6-ynoate (1.5 g, 4.48 mmol) and 4-toluenesulphonic acid (0.1 g) in dry benzene (15 ml) was heated under reflux under dry nitrogen for 2 hours. The cooled mixture was diluted with ether and the organic phase was extracted with aqueous sodium bicarbonate. The aqueous phase was acidified and extracted with ether. The organic phase was washed with brine and dried over magnesium sulphate. The solvents were removed to give 0.95 g (76% of theory) of 2-bromo-7-phenyl-(2E)-hepten-6-ynoic acid as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931469
Source datasetuspto-grants-1990_06
ORD IDord-9a0a02e5114c4162a2a29d97b461a5ee
Source noteuspto-grants-1990_06