HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 7-Bromo-4,4-dimethylthiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 18768217 | HCID 18768217 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Bromo-4,4-dimethylthiochroman | HCID 22393099 | 90.5% |
Reaction Steps
25.00 g (97.0 mmol) of 1-bromo-3-(3-methylbut-2-enylsulphonyl)benzene, 200 ml of toluene and 27.75 g (146.0 mmol) of para-toluenesulphonic acid are introduced into a three-necked flask. The reaction medium is refluxed for four hours and evaporated to dryness. The residue is taken up in aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with heptane. 22.57 g (90%) of the expected compound are obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148245B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-ef75afe850a246058183ba50cc54a66d |
| Source note | uspto-grants-2006_12 |