Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | HCID 53739243 | HCID 53739243 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 12672451 | HCID 12672451 | — |
Reaction Steps
To a solution of this 1-(4-methoxyphenyl)-3-methylthio-2-hexen-1,5-dione (2.0 g, 7.57 mmol) in 1,2-dichloroethane (20 ml) was added tetrafluoroboric acid (10 ml, 48%). The mixture was stirred for four hours at 50° C. during which time a dense yellow solid formed. After addition of water (25 ml) and filtration, crystallization from acetic acid gave pale yellow needles of 2-methyl-4-methylthio 6-(4-methoxyphenyl)pyrylium tetrafluoroborate: 2.2 g (87%), m.p. 207°-210° C. (decomp), IR (KBr)νCO +1625 cm-1 ; NMR(DMSO-d6)δ8.34 (s,1, aromatic), 8.29 (d,2, J=9.0 Hz, aromatic), 7.80 (br. 3, 1, aromatic), 7.18 (d, 2, J=9.0 Hz, aromatic) 3.97 (s, 3, OCH3), 2.91 (s, 3, SCH3), (s, 3, CH3); M.+ 246 (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04451659 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-9d7628d55adf489db1e56d99ca56a190 |
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| Source note | uspto-grants-1984_05 |
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