HuagongsheHuagongshe Chemistry Print Report · For research reference only
2',4'-Dihydroxyacetophenone → HCID 69411916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| Reactant | Ethyl 3,5-dimethoxybenzoate | HCID 87026 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69411916 | HCID 69411916 | — |
Reaction Steps
A solution of 20% lithiumhexamethyldisilazane in tetrahydrofuran (144 mL, 172 mmol), 2,4-dihydroxy acetophenone, 14 (6.5 g, 43 mmol) in tetrahydrofuran (150 mL) and ethyl-3,5-dimethoxy benzoate, 6 (9 g, 43 mmol) in tetrahydrofuran (100 mL) were reacted to afford 20, 1-(3,5-dimethoxy-phenyl)-3-(2,4-dihydroxy-phenyl)-propane-1,3-dione (15 g), which was cyclized with Dowex-H+ (5 g) in 2-propanol (200 mL) in a similar way as described for 22 to afford 26. Yield 7.6 g (59%); mp 267-268° C.; MS (FAB) 299 (M++1); IR (KBr) 3405, 1602; 1H NMR (200 MHz, DMSO-d6) δ 10.82 (s, 1H), 7.89 (d, J=8.7 Hz, 1H), 7.17 (d, J=2.0 Hz, 2H), 7.03 (d, J=1.9 Hz, 1H), 6.95 (s, 1H), 6.94 (dd, J=7.2 Hz, 2.0 Hz, 1H), 6.71 (s, 1H), 3.85 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07635779B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-6bd9b4bcb55d4ae6bd804e11356ecc2e |
| Source note | uspto-grants-2009_12 |