Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl acetylenedicarboxylate | HCID 12980 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | p-(Trifluoromethoxy)phenol | HCID 70015 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67749512 | HCID 67749512 | 70% |
Reaction Steps
A mixture of 4-(trifluoromethoxy)phenol (2.75 g, 12.5 mmole) and dimethyl acetylene dicarboxylate (1.69 ml, 13.7 mmole) in dioxane is treated with benzyltrimethylammonium hydroxide (0.15 ml, 40% aqueous) at room temperature under a nitrogen atmosphere, heated to 90°-95° C. (condensation complete by thin layer chromatographic analysis) cooled to 40° C. treated with sodium hydroxide (10 ml, 20% aqueous), heated at 90° C. for 1 hour and cooled to room temperature. The reaction mixture is treated with 10% aqueous HCl to pH 7 and filtered. The filtrate is acidified to about pH 1 with HCl to afford a yellow precipitate. The solid is filtered and dried to give the title product, 2.56 g (70% yield), mp 208°-210° C., identified by 1H, 13C and 19FNMR, mass spectral and elemental analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05681968 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-9c2763c616f64d85afc60bebe25c21f0 |
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| Source note | uspto-grants-1997_10 |
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