HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241509Generated: October 31, 2026
Pyridine → 3-iodo-6,7,8,9-tetrahydrobenzocylohepten-5-one-O-methyl-oxime
https://huagongshe.com/reaction/241509
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 3-Iodo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one | HCID 68296264 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-iodo-6,7,8,9-tetrahydrobenzocylohepten-5-one-O-methyl-oxime | HCID 123531255 | 97% |
Reaction Steps
To a stirred suspension of 3-iodo-6,7,8,9-tetrahydrobenzocylohepten-5-one prepared as described in example P3a (0.806 g; 2.82 mmol) in methanol (5.7 ml) was added pyridine (0.7 ml; 9.02 mmol) followed by a portion wise addition of methoxyamine hydrochloride (0.754 g; 9.02 mmol). The reaction mixture was stirred at 20° C. for 16 h under nitrogen. The solvent was removed in vacuo to afford 0.86 g (97% of theory) of crude 3-iodo-6,7,8,9-tetrahydrobenzocylohepten-5-one-O-methyl-oxime E/Z-mixture as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653003B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-88488df4619e45038cbaf9d37fa9c83f |
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| Source note | uspto-grants-2014_02 |
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