HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791045Generated: November 3, 2026
Triphenylphosphine → HCID 22042256, compound
https://huagongshe.com/reaction/1791045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 4-{[2-(iodomethyl)-2-propenyl]oxy}-3-formylbenzoate | HCID 22042282 | — |
| Reactant | Methyl 4-{[2-(chloromethyl)-2-propenyl]oxy}-3-formylbenzoate | HCID 22042284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22042256 | HCID 22042256 | 54% |
Reaction Steps
333 mg (1 mmol) of a 60/40 mixture of methyl 4-{[2-(iodomethyl)-2-propenyl]oxy}-3-formylbenzoate and of methyl 4-{[2-(chloromethyl)-2-propenyl]oxy}-3-formylbenzoate and then 297 mg (1.133 mmol) of triphenylphosphine are successively introduced into the 50 ml single-necked flask. The combined mixture is subjected to a stream of nitrogen and then 20 ml of acetonitrile are introduced via a hollow tube. After complete dissolution, the solution is brought to reflux overnight. After cooling the solution, 0.23 ml (1 mmol) of a solution of sodium methoxide in methanol is added dropwise and the medium is stirred for a further one hour. After the usual treatments, 120 mg (54%) of methyl 3-methylene-2,3-dihydro-1-benzoxepin-7-carboxylate are obtained in the form of a white solid; 1H NMR (300 MHz, CDCl3): 7.95 (d, J=1.8 Hz, 1H), 7.82 (dd, J=1.8 Hz and 8.4 Hz, 1H), 7.01 (d, J=8.4 Hz, 1H), 6.51 (d, J=12 Hz, 1H), 6.38 (d, J=12 Hz, 1H), 5.28 and 5.11 (2s, 2H), 4.61 (s, 2H), 3.89 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071340B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-f5df823ed3eb434a8e25c7760acc0ac2 |
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| Source note | uspto-grants-2006_07 |
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