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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791045Generated: November 3, 2026

Triphenylphosphine → HCID 22042256, compound

https://huagongshe.com/reaction/1791045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 4-{[2-(iodomethyl)-2-propenyl]oxy}-3-formylbenzoateHCID 22042282—
ReactantMethyl 4-{[2-(chloromethyl)-2-propenyl]oxy}-3-formylbenzoateHCID 22042284—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 22042256HCID 2204225654%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071340B2
Source datasetuspto-grants-2006_07
ORD IDord-f5df823ed3eb434a8e25c7760acc0ac2
Source noteuspto-grants-2006_07