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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353178Generated: October 30, 2026

Sodium Hydroxide → 57962-58-0

https://huagongshe.com/reaction/1353178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 21102633HCID 21102633—
SolventTetrahydrofuranHCID 8028—
Product57962-58-0HCID 2171402730%

Reaction Steps

6 ml of tetrahydrofuran (THF) and 3.5 mmol of 1-benzyl-4-(1-phenyl-2,2-dimethoxyethylamino)-(S,S)-3,5-bis(1-methoxyethyl)-1,2,4-triazolium bromide are introduced into a 100 ml round-bottomed flask equipped with a reflux condenser and a magnetic stirrer and then 1.75 ml of a 2 mol/l solution of lithium borohydride in THF are added at ambient temperature over a period of 1 to 2 h approximately. The reaction medium is subsequently left stirring at ambient temperature for 3 h and then brought to reflux for 3 h. After returning to ambient temperature, 20 ml of a 20% aqueous sodium hydroxide solution are added and then the aqueous phase is extracted with dichloromethane. The resulting organic phase is dried over anhydrous magnesium sulphate and then concentrated. The amine is purified by distillation. 0.19 g of the expected compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220883B2
Source datasetuspto-grants-2007_05
ORD IDord-bcec862df84447dc855c4ed33cf0446c
Source noteuspto-grants-2007_05