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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722234Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 86743282, compound

https://huagongshe.com/reaction/1722234

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 numberUS04855086
Source datasetuspto-grants-1989_08
ORD IDord-6225af415b5e4ccbbf0ab12a0267e19a
Source noteuspto-grants-1989_08