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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790839Generated: October 30, 2026

Benzyl Bromide → Cromolyn

https://huagongshe.com/reaction/1790839

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 numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-a071dfd71506458a9bb2d41efffdf7a2
Source noteuspto-grants-2006_07