HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436032Generated: October 31, 2026
Chlorotrimethylsilane → 1H-Isoindole-1,3(2H)-dione, 2-(trimethylsilyl)-
https://huagongshe.com/reaction/436032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1H-Isoindole-1,3(2H)-dione, 2-(trimethylsilyl)- | HCID 82615 | — |
Reaction Steps
250 g (1.7 moles) of phthalimide were suspended in 2.75 liter of acetonitrile and after 250 ml (1.8 moles) of triethylamine were added, the mixture was heated to gentle reflux 250 ml (1.97 moles) of trimethylchlorosilane were added in 10 minutes and the reaction mixture was then concentrated to a thick paste. 2.5 liter of light petroleum (80°-110° C) were added, the triethylammonium hydrochloride was filtered off and washed with 500 ml of light petroleum. The filtrate and washings were combined and concentrated until crystallization started. After cooling in the refrigerator for several hours, N-trimethylsilylphthalimide was isolated by filtration, washed with a small portion of light petroleum (40°-60° C) and dried in vacuo. The compound was further purified by recrystallization from ligroin (80°-100° C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04007202 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-8695643139344fe3a8c9bdb4e7da27ac |
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| Source note | uspto-grants-1977_02 |
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