HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433360Generated: October 28, 2026
Trimethylsilyl iodide → HCID 22312334, compound
https://huagongshe.com/reaction/433360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 12593302 | HCID 12593302 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22312334 | HCID 22312334 | — |
Reaction Steps
Step D—Removal of the Methoxyoxvcarbonyl Group (MOC): To the 4-methoxycarbonylamino-1,2,3,4-tetrahydroisoquinoline-3-one (3,4 mmoles) in 30 mL of acetonitrile was added 2 mole equivalents of trimethylsilyliodide (TMSI). The reaction mixture was heated to 50-80° C. for 3 hrs and then cooled and poured into a seperatory funnel. The reaction mixture was diluted with ethyl acetate and washed with 1 molar K2CO3 and then with 5% NaHSO3. The organic layer was dried over Na2SO4 and filtered. The solvent was removed under reduced pressure to give the 4-amino-1,2,3,4-tetrahydroisoquinoline-3-one derivative. Typical yields range from 50-87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06667305B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-96cc6c572bb4433ab28fe436221f35a6 |
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| Source note | uspto-grants-2003_12 |
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