HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 22419897, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 22419891 | HCID 22419891 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22419897 | HCID 22419897 | 87.1% |
Reaction Steps
To a stirred solution of 1,3-dihydro-6-fluoro-2,1-benzisothiazole-2,2-dioxide (2.57 g) in anhydrous pyridine (8 ml) was added ethyl chloroformate (1.79 g) at 0° C. under N2 atmosphere. The mixture was stirred for 30 minutes and concentrated in vacuo. Cold hydrochloric acid was added to the precipitate (pH=6). The resulting solution was extracted with ethyl acetate. The organic layer was washed with water and dried over magnesium sulfate. The crude product was purified by silica gel column chromatography (methylene chloride-ethyl acetate 95:5) to give 1-ethoxycarbonyl-1,3-dihydro-6-fluoro-2,1-benzisothiazole 2,2-dioxide (3.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05504095 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-2e5ae54318224027b47ac6bfe97c1c87 |
| Source note | uspto-grants-1996_04 |