HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 5-(2-Chloroethyl)Oxindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 5-(Chloroacetyl)-1,3-dihydro-2H-indol-2-one | HCID 2060576 | — |
| Product | 5-(2-Chloroethyl)Oxindole | HCID 14581392 | — |
Reaction Steps
To a 100 ml round-bottomed flask equipped with condenser and N2 inlet were added 5.0 g (23.9 mmol) of 5-chloroacetyl oxindole and 18.5 ml trifluoroacetic acid. To the stirring solution was added 8.77 ml (54.9 mmol) of triethylsilane while cooling to prevent exotherm, and the reaction stirred 16 hours at room temperature. The reaction was then poured into ice water, stirred, and the beige solid filtered, washed with water and hexane, and dried to give 5-(2-chloroethyl)oxindole, m.p. 168°-170° C., 3.0 g (64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831031 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-9312f3ed741947a3bc366c4b5fc5631a |
| Source note | uspto-grants-1989_05 |