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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455974Generated: November 1, 2026

Sodium Bicarbonate → methyl 2-[N-(2-hydroxy-5-bromobenzyl)-N-ethylamino]pyridine-5-carboxylate

https://huagongshe.com/reaction/1455974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl acetate hexaneHCID 21226206—
Reactantmethyl 2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridine-5-carboxylateHCID 22622546—
SolventDichloromethaneHCID 6344—
Productmethyl 2-[N-(2-hydroxy-5-bromobenzyl)-N-ethylamino]pyridine-5-carboxylateHCID 1172823075.1%

Reaction Steps

A solution of methyl 2-(N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]-5-pyridylcarboxylate (10.0 g, 22 mM) in dichloromethane (150 ml) was treated with boron trichloride dimethyl sulfide complex (40 ml, 2M, 80 mM). The reaction was stirred at ambient temperature for 48 hours. Saturated sodium bicarbonate solution was added and the layers were separated. The aqueous layer was washed with dichloromethane. The organic layers were combined, dried (MgSO4) and evaporated to give an off-white solid. The off-white solid was subjected to chromatography (diluted with ethyl acetate/hexane) to give the title product methyl 2-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]-pyridine-5-carboxylate (6.02 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843942
Source datasetuspto-grants-1998_12
ORD IDord-3cc0a18728634f7c9c339f7ef6a0b696
Source noteuspto-grants-1998_12