Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901051Generated: November 3, 2026

Hydrochloric Acid → HCID 23370072, compound

https://huagongshe.com/reaction/1901051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluorideHCID 6356—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamideHCID 23370116—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23370072HCID 2337007268.2%

Reaction Steps

To a suspension of sodium borohydride (2.72 g) in tetrahydrofuran (80 ml) was added dropwise under ice-cooling BF3, Et20 (8.86 ml) and the mixture was stirred for 30 minutes. To this mixture was added by portions N-(2-aminophenyl )-3,5-di-t-butyl-4-hydroxybenzamide (3.06 g ) and the mixture was stirred overnight while returning slowly to room temperature. 6N hydrochloric acid war added and the mixture was heated under reflux for 30 minutes, the solvent was distilled off and the residue was placed into water, neutralized with sodium hydrogen carbonate, extracted with ethyl acetate, washed with water and saturated saline and dried over anhydrous MgSO4. The solvent was distilled off and the residue was purified by a silica gel column chromatography (hexane:ethyl acetate=4:1) to give (2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzylamine (2.00 g, 68%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576335
Source datasetuspto-grants-1996_11
ORD IDord-5bf23823dd06442684d777b9a9816bfa
Source noteuspto-grants-1996_11