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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607258Generated: October 30, 2026

Ammonium Chloride → 2-(p-Methoxybenzyl)-3,7-dimethyl-4-hydroxy-5-propylbenzofuran

https://huagongshe.com/reaction/1607258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(p-Methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-7-dimethylaminomethylbenzofuranHCID 14570898—
SolventEthanolHCID 702—
Product2-(p-Methoxybenzyl)-3,7-dimethyl-4-hydroxy-5-propylbenzofuranHCID 1457089991.3%

Reaction Steps

To a solution of 2-(p-methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-7-dimethylaminomethylbenzofuran (0.2 gm; 0.54mmole) in ethanol (5 mL) was added sodium borohydride (0.2 gm, 5.45mmoles) and the reaction mixture was refluxed for 10 minutes. The reaction mixture was cooled, poured in a saturated solution of ammonium chloride, and extracted with ether. The organic phase was washed with with brine, dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed on silica gel using 20% ethylacetate in hexane as eluent to yield 160 mg (91%) of 2-(p-methoxybenzyl)-3,7-dimethyl-4-hydroxy-5-propylbenzofuran, mp. 102°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-87cac35ed6c6453d968d746d33c257fa
Source noteuspto-grants-1989_09