HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 22168678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Monomethyl-5-nitroisophthalate | HCID 6931682 | — |
| Reactant | 1-Methyl 3-(2-propen-1-yl) 5-amino-1,3-benzenedicarboxylate | HCID 22168580 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22168678 | HCID 22168678 | — |
Reaction Steps
Starting material (3(b)) was synthesised as follows. A mixture of mono-methyl-5-nitroisophthalate (13.8 g), allyl bromide (7.96 g), potassium carbonate (13.94 g) and DMF (160 ml) was stirred at ambient temperature for 4.5 h. The solid was filtered and DMF was evaporated away from the filtrate under reduced pressure. The residue was dissolved in diethyl ether (300 ml) and water (100 ml) and stirred for five minutes. The organic layer was separated and washed with saturated sodium bicarbonate solution (220 ml), brine (200 ml). dried over magnesium sulphate and evaporated under reduced pressure to give 5-nitro-isophthalic acid allyl ester methyl ester (3(a)) as a yellow oil (14.74 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541491B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-ccbf443955004c7b845c19a3ee27cb8c |
| Source note | uspto-grants-2003_04 |