HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → 2-trimethylsilyloxy-1H-indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Indanone | HCID 11983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-trimethylsilyloxy-1H-indene | HCID 10899736 | 72% |
Reaction Steps
30.3 g (0.30 mole) of triethylamine are added to a solution of 36.5 g (0.28 mole) of 2-indanone and 32.4 g (0.30 mole) of trimethylchlorosilane in 300 ml of tetrahydrofuran at room temperature while stirring. Stirring is continued for a further 3 hours at room temperature (20° C.), the precipitate which has separated out is filtered off under suction and the filtrate is evaporated down. The residue is purified by distillation (53° C., 0.3 mbar). 40.6 g (72%) of 2-trimethylsilyloxy-1H-indene are obtained as a colorless liquid in this manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250553 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-e4950c7830b24dec807c32d29028feaf |
| Source note | uspto-grants-1993_10 |