Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367311Generated: October 30, 2026

Ammonium Chloride → HCID 178430664, compound

https://huagongshe.com/reaction/367311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 178475393HCID 178475393—
SolventTolueneHCID 1140—
ProductHCID 178430664HCID 17843066437%

Reaction Steps

Under a nitrogen atmosphere, 0.98 g of 1-amino-3-[(5-acetoxy-4,6-di-t-butyl-2-methyl-2,3-dihydrobenzofuran-2-yl)methyl]guanidine was dissolved in 50 ml of toluene. To the solution was added 10 ml of diisobutyl aluminum hydride (1.0 M in toluene) and the mixture was stirred at room temperature for 1 hour. After reaction, a saturated aqueous ammonium chloride solution was added and insoluble matters were filtered off on Celite. The filtrate was extracted with ethyl acetate and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated. The concentrate was purified by silica gel column chromatography eluting with chloroform containing 10% methanol to give 0.32 g of 1-amino-3-[(4,6-di-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran-2-yl)methyl]guanidine as a white crystal (yield 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133279
Source datasetuspto-grants-2000_10
ORD IDord-292d3a22c74e4b62b891b756023efcca
Source noteuspto-grants-2000_10