HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromoethane → HCID 69033169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 7-Hydroxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one | HCID 5381920 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69033169 | HCID 69033169 | — |
Reaction Steps
This compound (58) was prepared from 7-hydroxy-3′,4′,5′-trimethoxy-flavone, 25 (2.3 g, 7 mmol), dibromo ethane (3 mL, 35 mmol) and potassium carbonate (2.9 g, 21 mmol) in dry dimethyl formamide (120 mL) using the identical procedure as described for 56. Yield 2.1 g (68%); mp 184-185° C.; MS (FAB) 435/437 (M++1); IR (KBr) 1631; 1H NMR (200 MHz, CDCl3) δ 8.15 (d, J=9.3 Hz, 1H), 7.10 (s, 2H), 7.01 (d, J=7.8 Hz, 1H), 6.99 (s, 1H), 6.71 (s, 1H), 4.43 (t, J=6.2 Hz, 2H), 3.96 (s, 6H), 3.93 (s, 3H), 3.70 (t, J=6.2 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07635779B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-bd1a01de0b2b4f1db115b03b2bc21d40 |
| Source note | uspto-grants-2009_12 |