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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489088Generated: October 29, 2026

Benzyl Bromide → Cromolyn

https://huagongshe.com/reaction/489088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Bis(2-carboxychromon-5-yloxy)-propan-2-ol disodium saltHCID 9827834—
SolventDimethylformamideHCID 6228—
ProductCromolynHCID 288270.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974802B2
Source datasetuspto-grants-2005_12
ORD IDord-394892eec6164426b6829df73faf4493
Source noteuspto-grants-2005_12