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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant3-Iodo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-oneHCID 68296264—
SolventMethanolHCID 887—
Product3-iodo-6,7,8,9-tetrahydrobenzocylohepten-5-one-O-methyl-oximeHCID 12353125597%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653003B2
Source datasetuspto-grants-2014_02
ORD IDord-88488df4619e45038cbaf9d37fa9c83f
Source noteuspto-grants-2014_02