Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Acetic acid, 2,2-dimethoxy-, methyl ester | HCID 66647 | — |
| Catalyst | Iodine | HCID 807 | — |
| Product | HCID 11429511 | HCID 11429511 | 93.9% |
Reaction Steps
25 g (0.186 mol) of methyl dimethoxyacetate are added to 27 ml (0.215 mol) of acetyl chloride at ambient temperature. 0.1 g (0.2 mol %) of diiodine are added and then the reaction mixture is stirred at 55° C. for 16 hours. The excess acetyl chloride is evaporated under vacuum and then the residue is dissolved in 100 ml of dichloromethane. 49 g (0.204 mol) of triphenylphosphine are added and then the reaction mixture is stirred at 37° C. for 3 hours. The solvents are evaporated and then the residue is crystallized from diisopropyl ether. 70 g of (methoxy(methoxycarbonyl)methyl)triphenylphosphonium chloride are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357819B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-7b9c6ca5a73a4fe9a7d41678b8c86144 |
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| Source note | uspto-grants-2013_01 |
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