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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350838Generated: November 2, 2026

Hydrochloric Acid → tert-Butyl 2-[2-(2-aminoethyl)phenoxy]-2-methylpropionate

https://huagongshe.com/reaction/350838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylamineHCID 6341—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyl 2-[2-(aminocarbonylmethyl)phenoxy]-2-methylpropionateHCID 21949727—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-[2-(2-aminoethyl)phenoxy]-2-methylpropionateHCID 21949731—

Reaction Conditions

Temperature50 °C

Reaction Steps

tert-Butyl 2-[2-(aminocarbonylmethyl)phenoxy]-2-methylpropionate (1.4 g, 4.87 mmol) was dissolved in tetrahydrofuran (5.0 mL). Subsequently, under nitrogen atmosphere, borane-THF complex in THF solution [1,0M BH3-THF in THF (14.6 mL, 14.6 mmol)] was added thereto, the mixture was stirred for three hours at 50° C. Thereafter, concentrated hydrochloric acid was gradually added thereto at 0° C. The resultant mixture was stirred for one hour at room temperature and made basic with an aqueous ethylamine solution. Ethyl acetate was added thereto. The mixture was sequentially washed with water and brine, followed by drying over sodium sulfate. The mixture was subjected to concentration under reduced pressure and purification by silica gel column chromatography (chloroform/methanol=30/1), whereby the target compound was obtained (830 mg, 2.97 mmol, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183295B2
Source datasetuspto-grants-2007_02
ORD IDord-a0cf2c56be154994939d38a77f893097
Source noteuspto-grants-2007_02