HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → Benzo[b]thiophene-5-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(1-Benzothiophen-5-yl)malonic acid | HCID 57615041 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Benzo[b]thiophene-5-acetic acid | HCID 11469582 | 98.3% |
Reaction Steps
To xylene (2 mL) suspension of 0.10 g of 2-(1-benzothiophen-5-yl)malonic acid was added 4 mg of p-toluenesulfonic acid monohydrate, which was then refluxed for 1 hour. The solvent was distilled off under reduced pressure, and to the resultant residue was added cyclohexane. The precipitate was collected by filtration to provide 0.08 g of 2-(1-benzothiophen-5-yl)acetic acid as white solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273902B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-d153fde41fd2405e971d797d8234b1e8 |
| Source note | uspto-grants-2012_09 |