HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid | HCID 19603694 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride | HCID 19603831 | — |
Reaction Steps
A solution of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid (5.0 g) and thionyl chloride (12.1 ml) in tetrahydrofuran (50 ml) was stirred at 50° C. for 2 hours. After the solution was cooled to room temperature, the resulting precipitates were collected by filtration and washed with diisopropyl ether to give 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride (5.57 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994378 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-648fb067932a4e0b92fd92299ea25dda |
| Source note | uspto-grants-1999_11 |