HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Cromolyn
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Bis(2-carboxychromon-5-yloxy)-propan-2-ol disodium salt | HCID 9827834 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cromolyn | HCID 2882 | 70.6% |
Reaction Steps
1,3-bis(2-carboxychromon-5-yloxy)-propan-2-ol disodium salt (2.5 g, 5,2 mmol), was suspended in DMF. To the suspension was added benzyl bromide (0.734 ml, 6.2 mmol) and the reaction was kept overnight under stirring. An additional portion of benzyl bromide (0.734 ml, 6.2 mmol) was added. After 24 hr, the reaction mixture was poured into sodium hydrogen carbonate aqueous solution and extracted dichloromethane. The organic phase was washed with water two times and evaporated to give the dibenzyl ester of 1,3-bis(2-carboxychromon-5-yloxy)propan-2-ol (1.72 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06974802B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-394892eec6164426b6829df73faf4493 |
| Source note | uspto-grants-2005_12 |