Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902673Generated: November 1, 2026

Sodium borohydride → HCID 70532723, compound

https://huagongshe.com/reaction/1902673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20482609HCID 20482609—
ReactantHCID 70531914HCID 70531914—
SolventMethanolHCID 887—
ProductHCID 70532723HCID 70532723—

Reaction Steps

5.0 g. of sodium borohydride, (0.131 moles) is added portionwise to a solution of 13 g. (0.032 moles) of 4-(3-methylphenoxy)-1-[3-(N,N-diphenylamino)propyl]pyridinium iodide in 200 ml. of methanol over a 10 minute period, allowing the temperature to reach reflux. The reaction is refluxed another 20 minutes. Solvent is evaporated. The residue is dissolved in chloroform, washed with sodium carbonate solution, and dried. Solvent is evaporated. The residue is converted to the maleate in ether and recrystallized from acetonitrile to give 10.9 g. of 3,5-dihydro-4-(3-methylphenoxy)-N,N-diphenyl-1(2H)-pyridinepropanamine butenedioate (1:1), mp. 164°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364954
Source datasetuspto-grants-1982_12
ORD IDord-a0416846cb8e4bb5aea5ad3d530edc69
Source noteuspto-grants-1982_12