HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 16749113, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-4-hydroxy-5-methoxybenzoic acid | HCID 44215 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 16749113 | HCID 16749113 | — |
Reaction Steps
A mixture of 5-chloro-vanillic acid (4.05 g, 20 mmol), benzyl bromide (8.55 g, 50 mmol) and potassium carbonate (6.90 g, 50 mmol) in DMF (60 mL) was stirred at room temperature for 18 hours. The mixture was transferred into a separation funnel and ethyl acetate (100 mL) and water (100 mL) were added, the organic layer was separated, washed with water (2×50 mL) and brine (50 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was crystallised from dichloromethane/hexane. Yield: 7.34 g (96%) colourless needles. 1H-NMR (400 MHz, CDCl3) δ=3.92 (s, 3H, —OCH3), 5.13 (s, 2H), 5.36 (s, 2H), 7.31-7.51 (m, 10H), 7.53 (d, J=2.0 Hz, 1H), 7.73 (d, J=2.0 Hz, 1H). LRMS (FAB+): 91.0 (100), 382.1 (15, [M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361677B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-994c099e38074516b0ac7cda60a16bcd |
| Source note | uspto-grants-2008_04 |