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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647148Generated: October 24, 2026

Hydrochloric Acid → 3'-(Benzyloxy)-2-isopropylamino-acetophenone hydrochloride

https://huagongshe.com/en/reaction/647148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantIsopropylamineHCID 6363—
Reactant1-(3-(Benzyloxy)phenyl)-2-bromoethanoneHCID 88031—
SolventEthanolHCID 702—
Product3'-(Benzyloxy)-2-isopropylamino-acetophenone hydrochlorideHCID 20134461—

Reaction Steps

In 425 ml of ethanol, 64 g of 3-benzyloxyphenacyl bromide and 212 ml of iso-propylamine are stirred at 5° C. under N2 atmosphere, and the temperature is allowed to rise to 12° C. After 0.75 minutes, the clear solution is poured into 2 liters of crushed ice containing 500 ml of concentrated HCl and 1.5 liters of H2O. The mixture is stirred for 20 minutes, filtered and the solid is washed with water to afford 3'-(benzyloxy)-2-isopropylamino-acetophenone hydrochloride, mp 213°-215° C. dec.. A 5 g-sample of this material is stirred in 50 ml of methanol, and the mixture is cooled in ice and neutralized with 10% NaOH until a clear solution is obtained. To this solution, 2 g of NaBH4 is added and after 0.75 hours of stirring, the mixture is evaporated in vacuo, and the resulting solid is collected and washed with H2O. This gives, after drying, 4.4 g of m-(benzyloxy)-α-[(isopropylamino)methyl]benzyl alcohol, mp 83°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407819
Source datasetuspto-grants-1983_10
ORD IDord-d06a27a74e514d67a12d24ed9c4c6676
Source noteuspto-grants-1983_10