HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822100Generated: November 2, 2026
Triethylsilane → 5-(2-Chloroethyl)-6-chlorooxindole
https://huagongshe.com/reaction/1822100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 16128890 | HCID 16128890 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-(2-Chloroethyl)-6-chlorooxindole | HCID 10609474 | 100.1% |
Reaction Steps
A 2 L round-bottom flask is loaded with 300 g (1.22 mols) of 6-chloro-5-(2-chloro-1-hydroxy-ethyl)-1,3-dihydro-indol-2-one and 1140 ml of trifluoroacetic acid, under nitrogen atmosphere. The mixture is stirred at room temperature for 1 h, then heated to about 35-40° C. 214 ml (1.34 mols) of triethylsilane are then dropped therein in approx. 1 hr 30 min, keeping stirring for 12-14 h. Separately, a round-bottom flask is loaded with 3000 g of a water/ice mixture and the reaction mixture is carefully dropped therein, in about 1 hr 30 min, under strong stirring. The resulting white suspension is stirred for 30 min, then filtered, washed with purified water (4×500 ml) and heptane (400 ml), then dried at 60° C. under vacuum to afford 281 g of 6-chloro-5-(2-chloro-ethyl)-1,3-dihydro-indol-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07608711B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-9e9a28cac672496b8725c5ab12739d9f |
|---|
| Source note | uspto-grants-2009_10 |
|---|